61. Conditions And Diseases: Genetic Disorders: Craniofrontonasal Dysplasia Health and Home. craniofrontonasal dysplasia. htbinpost/Omim/dispmim?304110.craniofrontonasal dysplasia. Last Update Mon May 10 2004. http://www.health-home.net/Conditions_and_Diseases/Genetic_Disorders/Craniofront

Health and Home Craniofrontonasal Dysplasia HOME LOGIN ADD A LINK MODIFY A LINK ... PARTNER Looking for something in particular? the entire directory only this category Home Conditions and Diseases Genetic Disorders : Craniofrontonasal Dysplasia LINKS: National Library of Medicine: CNFS Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome252.html NORD: Craniofrontonasal Dysplasia Offers a general discussion and resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Craniofrontonasal%20Dysplasia OMIM: National Center for Biotechnology Information A clinical synopsis of Craniofrontonasal Dysplasia. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110 Craniofrontonasal Dysplasia Last Update: Mon May 10 2004

62. Healthwise Topic craniofrontonasal dysplasia, Back to previous page. SynonymsDisorder Subdivisions General Discussion Resources National http://www.stlukes-sf.org/health/healthinfo/index.cfm?section=healthinfo&page=ar

63. Frontonasal Dysplasia A. Oculoauricular-vertebral spectrum. B. Frontofacionasal dysostosis – autosomalrecessive inheritance. C. craniofrontonasal dysplasia. VII. Resources. http://www.genesoc.com/counseling/Outlines/frontonasaldysplasia.htm

Resources for Genetic Counselors site updated May 10, 2004 outlines links search Frontonasal Dysplasia (Median Cleft Face Syndrome) I. Contracting A. How have things been going since your last visit? B. What questions or concerns would you like to address today? II. Interim History A. Which physicians are you seeing? When are your follow-up appointments scheduled? B. Recent tests: video swallowing study, audiologic evaluation, O saturation studies? C. How have things been going since the cleft palate repair? Any complications? Current feeding issues? D. Developmental assessment questions Rolling over? Sitting when supported? Pincher grasp? Reaching for objects? Babbling? Any consonant sounds? Words? E. Are you satisfied with OT/PT services? Have you noticed improvements? III. Psychosocial Assessment A. Who lives in the home with you? B. Are you working outside the home? Who cares for him when you are at work? C. Do you have any help with his care? Do you feel like you need help? D.

64. Free Genealogy Search :: Health : Conditions_and_Diseases : Genetic_Disorders : NORD craniofrontonasal dysplasia Offers a general discussion andresources. » OMIM National Center for Biotechnology Information http://www.lineages.co.uk/dwodp/index.php/Health/Conditions_and_Diseases/Genetic

@import url( http://www.lineages.co.uk/wp-layout.css ); Genealogy Search :: Health : Conditions_and_Diseases : Genetic_Disorders : Craniofrontonasal_Dysplasia : Genealogy Links Directory Search: search the entire directory search this category only Top Health See also: Health: Conditions and Diseases: Rare Disorders National Library of Medicine: CNFS - Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. NORD: Craniofrontonasal Dysplasia - Offers a general discussion and resources. OMIM: National Center for Biotechnology Information - A clinical synopsis of Craniofrontonasal Dysplasia. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The content of this directory is based on the Open Directory and may have been modified by DWodp Powered by DWodp live Main Menu: Main Index Free Query Forums Genealogy Links FAQ ... Contact Search: Our Favorite Links: Origins.net Introduction to Scottish Family History Using LDS resources United Kingdom Tracing your Scottish Ancestry ... Scotlands People Categories: General Archives: February 2004 January 2004 December 2003 Meta: RSS .92

65. Orthopaedic Syndromes First Page deafnesshand syndrome; craniofrontonasal dysplasia; Craniometaphysealdysplasia; Craniosynostosis, Adelaide type; Craniosynostosis, type http://freeortho.com/syndromes.html

Orthopaedic Related Syndromes Orthopaedic related syndromes are listed below in alphabetical order. Click on the syndromes for further details: A B C D ... H I J K L M ... P Q R S T U V W X Y Z OMIM Database ALL Syndromes - Clinical Features University of Western Ontario - Paediatric Database Gene maping and Other details: Achondrogenesis Ib Achondrogenesis-hypochondrogenesis, type II Achondroplasia Acrocallosal syndrome ... XLA and isolated growth hormone deficiency

66. Diseases Coffin Lowry Syndrome. Costello Syndrome. Cowden Syndrome. craniofrontonasal dysplasia.CriglerNajjar Syndrome. Cystic Fibrosis. Camps. CFTR and Genetic Mutations. http://diseases.health.designerz.com/diseases-directory.php

Map.Designerz.com Diseases News Diseases Chat Diseases Site Map ... Mexico Web Intelligence about Diseases Designerz, L.L.C

67. Startplane /Health/Conditions_and_Diseases/Genetic_Disorders/Craniofrontonasal_D craniofrontonasal dysplasia. See also Top/Health/Conditions and Diseases/C. Links.NORD craniofrontonasal dysplasia Offers a general discussion and resources. http://www.startplane.com/Health/Conditions_and_Diseases/Genetic_Disorders/Crani

Start Plane About Us Free Webpages Top Health Craniofrontonasal Dysplasia Top Craniofrontonasal Dysplasia Sites Your Site Here! - Get your site listed on StartPlane! The #1 performance based directory online! See also: Top/Health/Conditions and Diseases/C Links NORD: Craniofrontonasal Dysplasia - Offers a general discussion and resources. National Library of Medicine: CNFS - Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. OMIM: National Center for Biotechnology Information - A clinical synopsis of Craniofrontonasal Dysplasia. This category needs an editor Last Updated: 2003-08-29 17:31:10 Search: search the entire directory search this category only Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The content of this directory is based on the Open Directory and may have been modified by DWodp Powered by DWodp pro Dominion Web

68. Lukol Directory - Health Conditions And Diseases Genetic Disorders Costello Syndrome (2). Cowden Syndrome (3). craniofrontonasal dysplasia (3).Cri du Chat Syndrome (5). CriglerNajjar Syndrome (5). Cystic Fibrosis (185). http://www.lukol.com/Top/Health/Conditions_and_Diseases/Genetic_Disorders/

Lukol Directory - Health Conditions and Diseases Genetic Disorders ... Your Genes, Your Health The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed. http://www.ygyh.org Gene Clinics Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. http://www.geneclinics.org IMMD Institute of Medical Molecular Diagnostics Ltd. The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood. http://www.immd.de/ The UDGD Spot Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. http://www.camp-a-roo.com/UDGD/ Primary Ciliary Dyskinesia Information on a rare congenital disease. http://www.p-c-d.org/en/ Genetic and Rare Conditions Site Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. http://www.kumc.edu/gec/support/

69. Karger Publishers Copyright © 2002 S. Karger AG, Basel. goto top of outline Introduction. Craniofrontonasalsyndrome (CFNS) is a subgroup of craniofrontonasal dysplasia (CFND). http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

70. AOJ 52:58 "Ocular Aspects Of Craniofacial Disorders" syndromic synostoses but the most common craniosynostoses include Pfeiffer, Crouzon,Apert, SaethreChotzen, Jackson-Weiss and craniofrontonasal dysplasia. http://www.aoj.org/abstracts/52/52_58.html

Am Orthopt J 52:58 (2002). John Pratt-Johnson Lecture Ocular Aspects of Craniofacial Disorders Ken K. Nischal, F.R.C., Ophth. Craniofacial disorders may comprise various entities such as clefting anomalies, tumors, e.g., fibrous dysplasia, orbito-facio-cranial trauma, and the craniosynostoses. Each may have significant ocular involvement but the focus of my discussion is the craniosynostoses. Craniosynostosis is the premature closure of one or more cranial sutures and this may be associated with systemic features or an isolated finding. When a suture closes prematurely growth of the skull continues parallel to the suture but is arrested or retarded perpendicular to it. This results in an irregular shape of the skull. Previously patients with suture synostosis were described as having a particular shaped head such as plagiocephaly, brachycephaly, or scaphocephaly to name a few. These are now better described in terms of the sutures involved, e.g., plagiocephaly is better described as unicoronal synostosis, brachycephaly as bicoronal synostosis, and scaphocephaly as sagittal synostosis. © 2002 The Board of Regents of the University of Wisconsin System Home Table of Contents Search

71. A Listing Of Disorders Corticobasal Degeneration. Costello Syndrome. craniofrontonasal dysplasia.Craniometaphyseal Dysplasia. Craniosynostosis, Primary. Cri du Chat Syndrome. http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm

Brain and Tissue Bank University of Maryland, Baltimore C C Syndrome Camptomelic Syndrome Carbamyl Phosphate Synthetase Deficiency Carbohydrate deficient Glycoprotein Syndrome Type Ia Carboxylase Deficiency, Multiple Carcinoid Syndrome Cardio Auditory Syndrome Cardiofaciocutaneous Syndrome Carnitine Deficiency Syndromes Carnitine Palmitoyltransferase Deficiency Carnosinemia Caroli Disease Carpenter Syndrome Castleman's Disease Cat Eye Syndrome Cataract Dental Syndrome Cataracts Catel Manzke Syndrome Caudal Regression Syndrome Cavernous Hemangioma Cayler Syndrome Central Core Disease Central Hypoventilation Syndrome, Congenital Cerebellar Agenesis Cerebellar Degeneration, Subacute Cerebral Palsy Cerebro Oculo Facio Skeletal Syndrome Cerebrocostomandibular Syndrome Chandler's Syndrome Charcot Marie Tooth Disease CHARGE Association Chediak Higashi Syndrome Chiari Frommel Syndrome Chikungunya Cholangitis, Primary Sclerosing Cholecystitis Chondrocalcinosis, Familial Articular Choroideremia Choroiditis, Serpiginous Chromosome 1, Trisomy Chromosome 3, Monosomy 3p2

72. SearchBug Directory: Health: Conditions_and_Diseases: Genetic_Disorders 2) Congenital Urological Disorders (29) Cornelia De Lange Syndrome (4) CostelloSyndrome (2) Cowden Syndrome (3) craniofrontonasal dysplasia (3) Cri du Chat http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/Genetic_D

All Searches Auctions CompanyFinder Entertainment ... Travel Search the Web: Web Images Audio Files News Multimedia Shopping Open Directory Search: Featured Websites Cystic Fibrosis Book Store At WellnessBooks.com - wellnessbooks.com Comprehensive source to books on Cystic Fibrosis. Includes community boards and chat, book reviews and online ordering. Buy Genetic Disorders Products - bounce.deal-market.com We link to merchants which offer Genetic Disorders products for sale. Online Doctors - Ask Us Now! - kasamba.com Kasamba's variety of health experts- including Doctors, Specialists, Herbalists, Nurses and more- offer real help for affordable consultation fees- live via chat or e-mail! Buy Genetics Books At Amazon.com and Save! - booksellersnow.com Would you like to save on Genetics Books at Amazon and other stores? Compare prices at BookSellersNow.com! Our site continually proves that online shopping can be fun! Genetic Disorders Health Conditions and Diseases Go to Directory Home Categories Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Acoustic Neuroma ... Zellweger Syndrome Related Categories: Web Pages - ranked by popularity Your Genes, Your Health

73. Hum. Mol. Genet. -- Feldman Et Al. 6 (11): 1937 4 Cohen , MM , Jr ( 1979 ) craniofrontonasal dysplasia. 10 Kapusta , L. , Brunner,HG and Hamel, BCJ ( 1992 ) craniofrontonasal dysplasia. Eur. J. Pediatr.. http://hmg.oupjournals.org/cgi/content/full/6/11/1937

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Abstract of this Article PDF Version of this Article Email this article to a friend Similar articles found in: Hum. Mol. Genet. Online PubMed PubMed Citation Search PubMed for articles by: Feldman, G. J. Muenke, M. Alert me when: new articles cite this article Download to Citation Manager Human Molecular Genetics Pages A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22 Introduction Results Linkage between CFNS and X chromosome markers Clinical findings in CFNS families ... References A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22 George J. Feldman Deeann E. Ward Elisabeth Lajeunie-Renier Dolores Saavedra Nathaniel H. Robin Virginia Proud Laura J. Robb Vazken Der Kaloustian John C. Carey M. Michael Cohen, Jr Valerie Cormier Arnold Munnich Elaine H. Zackai Andrew O. M. Wilkie R. Arlen Price and Maximilian Muenke The Children's Hospital of Philadelphia, Division of Human Genetics and Molecular Biology, and Departments of Pediatrics, Genetics and Psychiatry, University of Pennsylvania School of Medicine

74. NORD Rare Disease - Medical Transcription At Medword Corneal Dystrophy Cornelia de Lange Syndrome Corticobasal Degeneration CostelloSyndrome Cowpox craniofrontonasal dysplasia Craniometaphyseal Dysplasia http://www.medword.com/rardisC.html

Medword Resources C This listing of rare diseases is provided for spelling reference. Clicking on the link will generate a new window and take you to NORD's home page, where you may search for an abstract of the disease or order a full text report of the disease. Please read the notice at the bottom of this page before using this list. A B C D ... Z Find on this page C C Syndrome Camptomelic Syndrome Cancer, Colon Cancer, Prostate ... Cytomegalovirus Infection Please Click HERE for a comma-delimited list of the rare diseases that you may add to your speller. List made available by express written permission of NORD - National Organization for Rare Disorders, Inc. Important: Please use the above list at your own risk. While we make every effort to ensure accuracy, we cannot be held responsible for errors in spelling or capitalization, or any circumstance that may result because of said error. In using the above list you also agree to never hold ANSO Consulting Inc. or Medword Medical Transcription responsible for any errors should they exist. Please Note: Medword Medical Transcription About Medword Contact Medword Customer Care FAQs ... Prevent ID Theft Medword eStore Ad Authentic WAVpedal Foot Pedal WAVpedal allows PC playback of most all digital voice recorder formats.

75. ORPHANET - Rare Diseases - Orphan Drugs Printing version, DISEASE craniofrontonasal syndrome teebi type, Synonym(s)Brachycephalofrontonasal dysplasia Teebi syndrome, No description is available, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1519

76. Mioti: Diseases + Conditions Information from the National Organization for Rare Disorders. NORD CraniofrontonasalDysplasia. Information from the National Organization for Rare Disorders. http://www.mioti.com/cat/condition/condition.asp?Cat=Dysplasia

77. PHP-Nuke Canada Site - Links http//www.fibrosingmediastinitis.com Fibrous dysplasia Support Online For thoseseeking support and information concerning the rare bone diseases fibrous http://www.phpnuke-ca.com/Links-Health__Conditions_and_Diseases__Rare_Disorders_

Login or Register [Home] [Downloads] [Feedback] ... Ajouter votre lien! May I suggest... Buy and sell links to your website! Who's Online There are currently, 58 guest(s) and member(s) that are online. You are Anonymous user. You can register for free by clicking here Languages Select Interface Language: Albanian Arabic Brazilian Catala Chinese Czech Danish Dutch English Euskara Finnish French Galego German Greek Hungarian Icelandic Indonesian Italian Macedonian Norwegian Polish Portuguese Romanian Russian Slovak Slovenian Spanish Swedish Thai Turkish Ukrainian Vietnamese Add your link You are her : /Health/Conditions_and_Diseases/Rare_Disorders/ Categories : Top Health Conditions and Diseases Aarskog Syndrome ... Health: Conditions and Diseases: Genetic Disorders Link in this category : National Organization for Rare Disorders, Inc. Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. http://www.rarediseases.org/ Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.

78. Redirect http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110

79. Healthcyclopedia Index - C Cor Pulmonale, Costello Syndrome. Costochondritis, Cowden Syndrome. CraniofrontonasalDysplasia, Craniosynostosis. Creutzfeldt Jakob Disease, CriglerNajjar Syndrome. http://www.healthcyclopedia.com/c.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... Contact Us Alphabetic Index - C Campylobacteriosis Campylobacter Pylori Canavan Disease Cancer ... Cytomegalovirus

80. ORPHANET - Rare Diseases - Orphan Drugs Contact, Order the Orphanet book, Printing version, DISEASE Craniofrontonasaldysplasia, ICD Q75.8, No description is available, MIM 304110, Clinical signs(32), http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1520

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 4     61-80 of 93    Back | 1  | 2  | 3  | 4  | 5  | Next 20