61. Pediatric Research -- Abstracts: Tanner Et Al. 9 (8): 611 ARTICLES. The natural history of the silverrussell syndrome a longitudinal study of thirty-nine cases. JM Tanner, H Lejarraga and N Cameron. http://www.pedresearch.org/cgi/content/abstract/9/8/611

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Submit correspondence regarding this article Similar articles found in: Pediatric Research Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Tanner, J. M. Cameron, N. Alert me when: new articles cite this article Download to Citation Manager ARTICLES The natural history of the Silver-Russell syndrome: a longitudinal study of thirty-nine cases JM Tanner, H Lejarraga and N Cameron The growth of 39 children with Silver-Russell syndrome has been followed for 1-13 years. Pregnancy and labor were normal; none of the 61 sibs had the syndrome. Height at referral (mean age 4.6 years) averaged 3.6 SD below the mean and remained at this level during subsequent growth. Bone age averaged 69 percent of normal at referral but caught up by puberty, which occurred at the normal time. Nineteen cases were treated with human growth hormone without lasting effect. There is no clear-cut distinction between the Silver and Russell syndromes; the name should be Silver-Russell. It is

62. Newsletter References Ranke MB, Lindberg A. Growth hormone treatment of short children born small for gestational age or with silverrussell syndrome results from KIGS (Kabi http://www.aap.org/sections/Endocrinology/references.htm

Section on Endocrinology References from Summer/Fall Newsletter GROWTH HORMONE SHOULD NOT BE ADMINISTERED ROUTINELY TO CHILDREN WITH SHORT STATURE DUE TO INTRAUTERINE GROWTH RETARDATION WHO ARE NOT CLASSICALLY GROWTH HORMONE DEFICIENT Allen W. Root, MD Departments of Pediatrics, Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, FL All Children's Hospital, St. Petersburg, Florida References Botero D, Lifshitz F. Intrauterine growth retardation and long-term effects on growth. Curr Opin Pediatr 11:340-347,1999. Chatelain P, Peretti N, Lapillonne A, Nicolino M, Salle B, et al. New insights into the postnatal growth of infants born "idiopathic' small for gestational age. J Pediatr Endocrinol Metab 14:1515-1519,2001. Coutant R, Carel J-C, Letrait M, Bouvattier C, Chatelain P, Coste J, Chaussain J-L. Short stature associated with intrauterine growth retardation: Final height of untreated and growth hormone-treated children. J Clin Endocrinol Metab 83:1070-1074,1998. de Zegher F. Growth hormone treatment in intrauterine growth retardation. 84th Annual Meeting of the Endocrine Society, San Francisco, CA, June 19-22, 2002, Abst S8-1, p 26.

63. SearchBug Directory: Health: Conditions_and_Diseases: S Shprintzen Syndrome (5) Shwachman Syndrome (7), ShyDrager Syndrome (4) Shyness (60) Sickle Cell Disease (20) SIDS (29) silver-russell syndrome (2) Sinusitis (27 http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/S/

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64. ADC -- Abstracts: Lai Et Al. 71 (6): 490 Archives of Disease in Childhood. PAPERS. Cognitive abilities associated with the silverrussell syndrome. KY Lai, D Skuse, R Stanhope http://adc.bmjjournals.com/cgi/content/abstract/archdischild;71/6/490

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles in ADC Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Lai, K. Hindmarsh, P Alert me when: new articles cite this article Download to Citation Manager PAPERS Cognitive abilities associated with the Silver-Russell syndrome KY Lai, D Skuse, R Stanhope and P Hindmarsh Department of Psychiatry, Prince of Wales Hospital, Shatin, Hong Kong. There is no consensus opinion on whether or not cognitive impairments are found in the Silver-Russell syndrome. An investigation of a substantial sample was undertaken, using standardised assessments, in 20 boys and five girls aged 6.0 years to 11.8 years. Mean (SD) birth weights were -2.65 (0.95) SD scores, corrected for gestation. At evaluation the children had a mean (SD) age of 8.8 (1.8) years and a mean height of -2.26 (1.5) SD scores. Tests of cognitive abilities included assessments of general intelligence, reading and arithmetic attainments, and a cognitive

65. ADC -- Abstracts: Davies Et Al. 63 (2): 130 of Disease in Childhood. PAPERS. Adolescent growth and pubertal progression in the silverrussell syndrome. PS Davies, R Valley and http://adc.bmjjournals.com/cgi/content/abstract/archdischild;63/2/130

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles in ADC Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Davies, P. Preece, M. Alert me when: new articles cite this article Download to Citation Manager PAPERS Adolescent growth and pubertal progression in the Silver-Russell syndrome PS Davies, R Valley and MA Preece Department of Growth and Development, Institute of Child Health, London. The pattern of growth and development of 18 adolescent children with the Silver-Russell syndrome was studied. Mature height was about -3.6 standard deviation scores in both sexes. This is comparable to the height reduction at diagnosis, which has been reported previously. The pattern of puberty and adolescent growth was essentially normal and occurred at a marginally earlier time than normal, although in this small series the differences were not significant. In the girls there was a tendency to gain subcutaneous fat after puberty. This trend was not apparent in the boys.

66. •¶Œ£ˆê—— Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, KanekoIshino T, Ishino F. No evidence of PEG1/MEST gene mutations in silver-russell syndrome patients. http://www.ishino.bio.titech.ac.jp/list.html

•¶Œ£ƒŠƒXƒg Kaneko-Ishino T, Kohda T, Ishino F. The regulation and biological significance of genomic imprinting in mammals. J Biochem (Tokyo). 2003 Jun;133(6):699-711. Ono R, Shiura H, Aburatani H, Kohda T, Kaneko-Ishino T, Ishino F. Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. Genome Res. 2003 Jul;13(7):1696-1705. Inoue K, Ogonuki N, Mochida K, Yamamoto Y, Takano K, Kohda T, Ishino F, Ogura A. Effects of Donor Cell Type and Genotype on the Efficiency of Mouse Somatic Cell Cloning. Biol Reprod. 2003 Jun 11 in press Ogura A, Inoue K, Ogonuki N, Lee J, Kohda T, Ishino F. Phenotypic effects of somatic cell cloning in the mouse. Cloning Stem Cells. 2002;4(4):397-405. Hikichi T, Kohda T, Kaneko-Ishino T, Ishino F. Imprinting regulation of the murine and human genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites. Nucleic Acids Res. 2003 Mar 1;31(5):1398-1406. Lee J, Inoue K, Ono R, Ogonuki N, Kohda T, Kaneko-Ishino T, Ogura A, Ishino F. Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells. Development. 2002 Apr 15;129(8):1807-1817.

67. Salisbury 312750. RubensteinTaybi (16p) (FISH). 180849. silver-russell syndrome (Mat UPD7). 180860. Smith-Magenis (17p) (FISH). 182290. Spinal and Bulbar Muscular Atrophy. http://www.cmgs.org/labdir/labs/salisbury.htm

updated Laboratory: Wessex Regional Genetics Laboratory Postal address: Salisbury Health Care NHS Trust Salisbury District Hospital Salisbury Wiltshire Contact 1: Contact 2: Telephone 1: Telephone 2: Fax: Email 1: Email 2: Home page: Dr John Harvey Dr David Robinson john.f.harvey@dial.pipex.com wessex.genetics@dial.pipex.com Disease service: OMIM reference number Achondroplasia Alpha-1-antitrypsin deficiency Amyloidosis (Finnish type) Aniridia (FISH) Autism (dup15q11-130 Beckwith-Wiedemann syndrome Breast /ovarian cancer : familial (BRCA1,BRCA2) Cat Eye syndrome (22q11) FISH Cerebellar ataxias Charcot Marie Tooth disease (1A,1B, X) Cystic Fibrosis Deafness, sensorineural Cx26 Di George, velocardiofacial (del 22q11)FISH DRPLA (Dentatorubral pallidoluysion atrophy) Duchenne / Becker Muscular Dystrophy Factor V Leiden Familial Adenomatous Polyposis coli Fragile X disease A and E (FMR1, FMR2) Friedreich ataxia Haemochromatosis Hereditary Non Polyposis Colon Cancer (HNPCC) Huntington Disease Hypochondroplasia (FGFR3) Leukaemia translocations Marfan syndrome Mitochondrial diseases Myoclonus epilepsy progressive type 1 (Baltic) Myotonic dystrophy Oculopharyngeal Muscular Dystrophy Prader-Willi / Angelman syndrome PTEN Rett syndrome Rubenstein-Taybi (16p) (FISH) Silver-Russell Syndrome (Mat UPD7) Smith-Magenis (17p) (FISH)

68. ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page Version pour Impression, MALADIE silver-russell, syndrome de, CIM Q87.1, Le syndrome de silver-russell associe un retard de croissance http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=813

69. ORPHANET® : Silver-Russell, Syndrome De Translate this page ORPHANET. Accès à la base de données Orphanet. silver-russell, syndrome de. Accès direct aux détails Résumé Le syndrome de Silver http://www.orpha.net/static/FR/silverrussell.html

Accès à la base de données Orphanet Silver-Russell, syndrome de Accès direct aux détails Résumé Texte(s) long(s) http://www.orpha.net/data/patho/FR/fr-silver.html Signes de la maladie CLINODACTYLIE DU 5EME DOIGT COINS DE LA BOUCHE TOMBANTS FACE TRIANGULAIRE PETITE TAILLE / NANISME RETARD DE CROISSANCE INTRA-UTERIN AGE OSSEUX RETARD ASYMETRIE CORPORELLE / HEMITROPHIE DIFFICULTE D'ELEVAGE FRONT BOMBE/BOSSES FRONTALES LEVRES MINCES/RETRACTEES ANOMALIE APPAREIL URINAIRE ANOMALIE DU COEUR FENTE PALATINE LUXATION DE HANCHE OREILLES BAS IMPLANTEES Mise à jour : 01/06/2004 Accès à la base de données Orphanet

70. Russell-Silver Syndrome,RSS,SRS,Russell Syndrome,Silver Syndrome,Silver-Russell also known as RSS Silver Russell syndrome SRS Russell syndrome Silver syndrome RussellSilver Dwarfism silver-russell Dwarfism Disorder Subdivisions Russell http://www.icomm.ca/geneinfo/rss.htm

Russell-Silver Syndrome,RSS,SRS,Russell Syndrome,Silver Syndrome,Silver-Russell Syndrome,Russell-Silver Dwarfism,Silver-Russell Dwarfism,Russell-Silver Syndrome X-linked,Partington Syndrome,Russell-Silver Syndrome,RSS,SRS,Russell Syndrome,Silver Syndrome,Silver-Russell Syndrome,Russell-Silver Dwarfism,Silver-Russell Dwarfism,Russell-Silver Syndrome X-linked,Partington Syndrome For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Russell-Silver Syndrome also known as: RSS Silver Russell Syndrome SRS Russell Syndrome Silver Syndrome Russell-Silver Dwarfism Silver-Russell Dwarfism Disorder Subdivisions Russell-Silver Syndrome, X-linked (Partington Syndrome) (as defined by the National Organization for Rare Disorders PRELIMINARY DRAFT This preliminary draft has not been approved by our medical advisors; therefore, its accuracy cannot be guaranteed. Verification of medical accuracy is pending. This is the most current information that NORD has available at this time. Russell-Silver Syndrome is a very rare genetic disorder characterized by growth delays before birth (prenatal or intrauterine growth retardation); overgrowth of one side of the body (hemihypertrophy or asymmetry); unusual characteristic facial features; and other physical abnormalities. Growth delays before birth affect both weight and linear growth.

71. Retard Développement Foetal : Sites Et Documents Francophones Translate this page guide ressources. silver-russell, syndrome de Par Dr Toutain A. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. http://www.chu-rouen.fr/ssf/pathol/retarddeveloppementfoetal.html

Retard développement foetal Menu général CISMeF Synonyme(s) MeSH Hypotrophie foetale Voir aussi nourrisson petit pour âge gestation Arborescence(s) retard développement foetal fetal growth retardation maladies appareil génital féminin et complications grossesse maladies et malformations congénitales, héréditaires et néonatales signes et symptômes, états pathologiques Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : Qualificatifs : diagnostic bibliographie RCIU : définition échographique [Par M. Maugey-Laulom B. Site éditeur mots clés : âge gestationnel biométrie diagnostic différentiel échographie doppler ... signes et symptômes type(s) : * cours bibliographie enseignement et éducation Biométries foetales [Par M. Grangé G. Site éditeur mots clés : âge gestationnel biométrie biométrie histoire ... échographie type(s) : * cours questions à choix multiple illustration médicale Prématurité et hypotrophie néonatale - - Examen Classant National : Question(s) 21 Module(s) 2 - [Par Pr Rambaud P (CHU de Grenoble, Service de Médecine Néonatale et Réanimation Infantile).

72. NORD - National Organization For Rare Disorders, Inc. General Discussion. RussellSilver syndrome is a very rare genetic disorder characterized by growth of symptoms associated with Russell-Silver syndrome vary greatly from case to http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Russell Silve

73. Search: - Info.co.uk Results for Russell Silver syndrome from Info.co.uk metasearch. Find better search results from the Web, Yellow Pages and White Pages quickly and easily! SILVERRUSSELLsyndrome Contact a Family http://dpxml.infospace.com/infocom.uk/results?otmpl=dog/webresults.htm&qkw=R

74. Russell-Silver Syndrome Russell Silver syndrome national and international resources, clinics with genetic counselors and geneticists RussellSilver syndrome. Russell-Silver syndrome Network. Division of MAGIC Foundation Association for Children with Russell-Silver syndrome, Inc. 22 Hoyt Street http://www.kumc.edu/gec/support/russell.html

Russell-Silver Syndrome Russell-Silver Syndrome Network Division of MAGIC Foundation 6645 W. North Ave. Oak Park, IL 60302 Phone: 708.383.0808 / 800-3-MAGIC-3 Fax: 708.383.0899 E-mail: mary@magicfoundation.org Web page: http://www.magicfoundation.org Association for Children with Russell-Silver Syndrome, Inc. 22 Hoyt Street Madison, NJ 07940-1604 Phone: (201) 377-4531 or (313) 242-2219 Fax: (201) 822-2715 c/o Jodi Zwain For families with children who have Russell Silver intrauterine growth retardation Also See: National organizations , resouces for genetic conditions or birth defects Dwarfism / short stature resources University of Kansas Medical Center To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments Revised November 8, 2002 Genetic Societies Clinical Resources Labs Clinics ... Search Genetics Education Center Debra Collins, M.S. CGC , Genetic Counselor, dcollins@kumc.edu This site subscribes to the principles of the HONcode (Health on the Net, Code of Conduct for Medical and Health Web Sites)

75. Russell-Silver Syndrome RussellSilver syndrome - A Story. I created this article for two distinct purposes. First, I wanted to have a way to inform those who were unaware of Russell-Silver syndrome. dwarfisms known to http://www.buradley.com/rss/rssstory.htm

Russell-Silver Syndrome - A Story I created this article for two distinct purposes. First, I wanted to have a way to inform those who were unaware of Russell-Silver syndrome. Second, and most important, I wanted to create an informative and concise summary of Russell-Silver syndrome for parents with newly born or diagnosed RSS children. I intend this article to an overview of the syndrome. If you want more detailed information on this subject, You can research more on your own. The bibliography located at the end of this manual can get you started on the right track. If, in the course of reading this manual, you run across words you don't know, please refer to the glossary at the end. You may wish to glance over the glossary first is you are unfamiliar with medical terminology related to dwarfism and Russell-Silver syndrome. Defining Russell-Silver Syndrome When the average American thinks of a dwarf, they usually picture a person with a normal sized torso and head, but with shortened limbs, looking like the characters from the movie Willow . This type of dwarfism, known as Acondroplasia, is only one of the nearly 300 diagnosable dwarfisms known to modern medicine. Russell-Silver syndrome is another type of dwarfism, although less common. Both Dr. A. Russell and Dr. H. K. Silver first diagnosed Russell-Silver syndrome (abbreviated RSS) separately in the mid 1960's. The two doctor's findings were later combined to one diagnoses. Sometimes doctors refer to Russell-Silver syndrome as Silver-Russell syndrome. I will get into the differences in these names later.

76. Russell Silver Syndrome - Information / Diagnosis / Treatment / Prevention The CaF Directory A definition of Silver Russell syndrome, its inheritance patterns, and prenatal diagnosing. Also lists a http://www.healthcyclopedia.com/genetic-disorders/russell-silver-syndrome.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... genetic disorders > russell silver syndrome Russell Silver Syndrome Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Related Topics Health News Web Directory: Related Topics: Rare Disorders Health News: Search millions of published articles for news on Russell Silver Syndrome Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: NORD: Russell Silver Syndrome Offers a general discussion, the synonyms and further resources. The CaF Directory A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. Also lists a support group in the United Kingdom. Notes: Healthcyclopedia presents health information in the form of websites and articles that encompass conventional medicine and alternative treatments Under no circumstances can it recommend or endorse a specific drug or therapy or treatment.

77. ► Russell-Silver Syndrome the body. Alternative Names Silver Russell syndrome; Silver syndrome. Causes, incidence, and risk factors Genetic problems are http://www.umm.edu/ency/article/001209.htm

Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Russell-Silver syndrome Overview Symptoms Treatment Prevention Definition: A condition of unknown origin, but which is characterized by short stature and frequent asymmetry in the size of 2 halves or parts of the body. Alternative Names: Silver Russell syndrome; Silver syndrome Causes, incidence, and risk factors: Genetic problems are thought to cause this syndrome although the specific gene(s) remain to be discovered. The pattern of inheritance has not been determined but in most cases it seems sporadic, that is to say, there is no family history in preceding generations/siblings. Children with Russell-Silver syndrome are born small and generally achieve less than 5 feet at adult height. Side-to-side asymmetry is fairly common, for example a left body part may be larger than the right counterpart. This asymmetry may occur anywhere including the face. Other findings include excessive sweating , a small triangular face which makes the skull look large by comparison, inward curving 5th fingers, and pigmented skin lesions called cafe-au-lait spots Review Date: 9/10/2001 Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

78. :: Ez2Find :: Russell Silver Syndrome The CaF Directory Site Info - Translate - Open New Window A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Russell Silver Syndrome Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Russell Silver Syndrome ez2Find Home Directory Health Conditions and Diseases ... Genetic Disorders : Russell Silver Syndrome Related Categories Health: Conditions and Diseases: Rare Disorders Web Sites The CaF Directory [Site Info] [Translate] [Open New Window] A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. Also lists a support group in the United Kingdom. URL: http://www.cafamily.org.uk/Direct/s30.html NORD: Russell Silver Syndrome [Site Info] [Translate] [Open New Window] Offers a general discussion, the synonyms and further resources. URL: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Russell%20Silver%20Syndrome%20%28RSS%29

79. Silver-Russellin Oireyhtymä Kehitysvammahuollon tietopankki. Sikiön pienikokoisuus, luuston epäkypsyys, seksuaaliset poikkeavuudet, kolmiomaiset kasvot, maitokahviläiskät http://www.saunalahti.fi/kup/syndroma/silver-russell.htm

Kehitysvammahuollon tietopankki Sikiön pienikokoisuus, luuston epäkypsyys, seksuaaliset poikkeavuudet, kolmiomaiset kasvot, maitokahviläiskät ja sormien epämuodostumat Silver-Russellin oireyhtymä Russell-Silverin oireyhtymä Russell-Silverin dwarfismi Oireyhtymä koostuu sikiöaikaisen kasvun vajavuudesta, syntymänjälkeisestä luuston kehityksen epäkypsyydestä, kasvun epäsymmetrisyydestä, seksuaalisen kehityksen poikkeavuudesta, pienistä kolmiomaisista kasvoista, ihon maitokahvimaisista läiskistä, sormijäsenten epämuodostumista, lantion tai kyynärpäiden sijoiltaan menoista ja muista epämuodostumista. Vammautuneen otsa on ulkoneva tai kohoava, alaleuka pieni ja kärjekäs. Kovakalvo (silmämunan valkoinen kerros) on sinertävä. Suu on suuri ja alakulmistaan alaspäin kääntynyt. Sormien ja varpaiden keskijäsenet ovat vajaakasvuiset aiheuttaen koukkuisuutta ja viidensien sormien vinoutumista. Raajojen pitkät luut ovat hontelot ja olkaluut lyhyet. Muita ominaisuuksia ovat verensokerin niukkuus, munuaistiehyiden happomyrkytystila, kasvaneet gonadotropiini-tasot (sukupuolihormonien eritystä sääteleviä hormoneja) ja toisinaan kasvuhormonin vähäisyys. Kasvun hidastuminen ja toisinaan psyykkinen kehitysvammaisuus ovat tyypillisiä piirteitä. Noin kolmanneksella vammautuneista lapsista on siittimen alahalkio ja piilokivekset. Virtsateiden poikkeuksia ovat vesimunuainen, virtsanjohtimien tukos, munuaisaltaan ja munuaisen tulehdus, virtsan takaisinvirtaus ja munuaisten laajentuma.

80. Russell Silver Syndrome Previews by Thumbshots The CaF Directory A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. http://www.oobdoo.com/directory/Health/ConditionsandDiseases/GeneticDisorders/Ru

World Wide Search Engine and Portal to the Best Sites on the Internet Over 15million sites and over 550,000 categories Top Health Conditions and Diseases Genetic Disorders : Russell Silver Syndrome (2) See Also: Health: Conditions and Diseases: Rare Disorders The CaF Directory - A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. Also lists a support group in the United Kingdom. NORD: Russell Silver Syndrome - Offers a general discussion, the synonyms and further resources. Back to ooBdoo Suggest a Site Feedback Link to ooBdoo ... Guarantee your site is listed This page also has modified,additions and deletions of information obtained from the Open Directory Project Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

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