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         Hemihypertrophy:     more detail
  1. Hemihypertrophy: Webster's Timeline History, 1885 - 2007 by Icon Group International, 2010-05-17
  2. Hemihypertrophy (Hemihyperplasia): An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005

81. Www.formudes.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemih
dwb.unl.edu/Teacher/NSF/C11/C11Links/www.sleeptight.com/EncyMaster/H/hemihypertrophy.html NodeWorks Genetic Disorders hemihypertrophy other. thumbnail, 1. DrHull - An article about hemihypertrophy,what it is, the features, follow up and prognosis. thumbnail, 2
http://www.formudes.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorder

82. Health Conditions And Diseases Genetic Disorders Hemihypertrophy
Health Conditions and Diseases Genetic Disorders hemihypertrophy Directoryresults Some web results for Genetic Disorders hemihypertrophy
http://world.ammissione.it/browse_/Health/Conditions_and_Diseases/Genetic_Disord
World Directory Health Hemihypertrophy Health Conditions and Diseases Genetic Disorders Hemihypertrophy
Directory results:
  • DrHull - An article about hemihypertrophy, what it is, the features, follow up and prognosis.
  • Hemihypertrophy - For patient and family, support and information regarding this disease. Related links and mailing list.
  • Hemihypertrophy - A description from International Birth Defects Information Systems.
Related sites for Hemihypertrophy:

83. Health: Conditions And Diseases: Genetic Disorders: Hemihypertrophy
www.surfrocket.com/Health/Conditions_and_Diseases/Genetic_Disorders/hemihypertrophy/ Istituto Giannina Gaslini Cell Bank hemihypertrophy - OMIM 235000. Code number, Disease, Sample type, Clinical phenotype,Family number. DNA2171994, hemihypertrophy, DNA, Affected, .. NA ..
http://www.san24.com/Health/Conditions_and_Diseases/Genetic_Disorders/Hemihypert
San24.com !
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  • DrHull Vorschau
    An article about hemihypertrophy, what it is, the features, follow up and prognosis.
    http://www.drhull.com/EncyMaster/H/hemihypertrophy.html
    (New: Sat Sep 06 2003
  • Hemihypertrophy Vorschau
    A description from International Birth Defects Information Systems.
    http://www.ibis-birthdefects.org/start/hemihype.htm
    (New: Sat Sep 06 2003
  • Hemihypertrophy Vorschau
    For patient and family, support and information regarding this disease. Related links and mailing list.
    http://www.geocities.com/HotSprings/Spa/6112 (New: Sat Sep 06 2003
Last update: Fri May 21 2004 - 21:09:33 - (322951) San24.com ! Give me Link ! Home Search Search suggestion Add URL ... New Links

84. Wuup.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemihypertrop
www.phatnav.com/directory/Health/Conditions_and_Diseases/Genetic_Disorders/hemihypertrophy.cat www.sweden.org/Health/Conditions_and_Diseases/Genetic_Disorders/hemihypertrophy/ Guests of the Hemi Web Site Visitor chris ceraso Reference hemihypertrophy website Location Sewell, nj WebSiteWeb Info Contact chrismagcer@comcast.net Date Fri, Apr 23, 2004 at 15
http://wuup.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemihy

85. NWTSG Patient Information Page
children with Wilms tumor registered in a national clinical trial during 196981showed high rates of aniridia, hemihypertrophy, cryptorchidism, hypospadias
http://www.nwtsg.org/public/patient_info.html
Welcome to the Wilms Tumor Patient Information Page
Questions Concerning Wilms Tumor?
    Send your questions to Guilio J. D'Angio, MD at the Radiation Oncology Hospital of the University of Pennsylvania, 3400 Spruce Street Philadelphia, PA 19104 Phone: 215/662-3074 Fax: 215/349-5949 email: sucher@xrt.upenn.edu

Articles on Wilms Tumor:
Some links that might help:
Publications of Interest:
  • Breslow NE, Beckwith JB: Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study. Journal of the National Cancer Institute 68(3): 429-436, 1982.
  • Nearly 2,000 children with Wilms' tumor registered in a national clinical trial during 1969-81 showed high rates of aniridia, hemihypertrophy, cryptorchidism, hypospadias, and other genitourinary anomalies. Patients with bilateral disease, who constituted 5% of the total, had younger ages at diagnosis and an increased incidence of congenital anomalies and renal blastemal rests. Those with multicentric unilateral lesions had more blastemal rests but were otherwise indistinguishable from the unicentric cases. The 20 familial cases had none of the features usually associated with genetic tumors: neither younger ages nor an increase in bilaterality nor associated congenital anomalies. These observations suggest that the fraction of Wilms' tumors that is due to an inherited mutation may be substantially smaller than previously supposed and support the concept that the disease arises from a variety of pathogenetic pathways. (Author abstract) (38 Refs)

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