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         Bardet-biedl Syndrome:     more detail
  1. Biochemists focus on BBS.(Michel Leroux and Oliver Blacque's research on Bardet-Biedl Syndrome ): An article from: Canadian Chemical News
  2. Bardet-Biedl Syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Avis Gibons, 2005
  3. Maladie Du Segment Postérieur: Dégénérescence Maculaire Liée à L'âge, Uvéite, Syndrome de Bardet-Biedl, Rétinite Pigmentaire (French Edition)
  4. The (Laurence Moon) Bardet Biedl syndrome (Van Gorcum's medical collection, no. 207) by W Stiggelbout, 1969

81. Laurence Moon Bardet Biedl Syndrome Network
Laurence Moon Bardet Biedl syndrome Network. 124 Lincoln Ave Purchase, NY 10577 ConditionsRetinitis Pigmentosa Laurence Moon Bardet Biedl syndrome.
http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Laur

82. Retina International's Scientific Newsletter - Bardet Biedl Syndrome Loci
Scientific Newsletter. Disease Database Bardet Biedl syndrome. Recent updatefrom 16.07.99 Disease, Genelocus, MIM, Gene, Gene MIM, MoI, Assignment.
http://www.retina-international.org/sci-news/bardet.htm
Retina International's Scientific Newsletter
Disease Database
Bardet Biedl Syndrome
Recent update from: 13.03.2003 Disease Genelocus MIM Gene Gene MIM MoI Assignment
Linked Marker [cM] Remarks References
BBS Polygenic
ar

  • Turns out to be a polygenic disease
  • Triallelic Inheritance by mutations in BBS2, BBS4, BBS6 gene has been shown
  • Synergistic effect of BBS2L1 and BBSL2
    type 1 ar
    PYGM- D11S913
    type 2 ar
    D16S2937-[2.69 cM-D16S408-441f2-5a3-291f1-D16S2938-D16S673-55019-405f3-152e5D16S3057]-152e5-700h13 type 3 ar type 4 ar
  • PDP
  • Bedouin
  • Italian type 5 ar pter-[~39 D2S442-[5]- D2S1399-[5]- D2S2241-[4]- D2S142- D2S418-[2.8]- D2S1353- D2S156-[13 [5]- D2S124- D2S330-[4]- D2S1776-[3]- D2S335-[1]- D2S1238]-[5]- D2S2314- D2S1391]-qter
  • Inbred Newfoundland family of European ancestry
  • PDP type 6 MKKS ar D20S115- 2,5 cM- [D20S851- MKKS- D20S189 20 cM]- 0,5 cM- D20S186
  • RP
  • Polydactyly
  • Obesity
  • Learning disability
  • Diabetes melitus
  • Renal anomalies type 7 ar MoI = Mode of Inheritance: a: autosomal, ad: autosomal dominant, ar: autosomal recessive, xl: x-linked, mt: mitochondrial References
  • Badano,J.L., Ansley,S.J., Leitch,C.C., Lewis,R.A., Lupski,J.R., and Katsanis,N. Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2. 2003; Am.J.Hum.Genet. 72: 650-658.
  • 83. Health Library - Bardet Biedl Syndrome
    Bardet Biedl syndrome. Disorder Subdivisions. None. General Discussion. BardetBiedlsyndrome is a rare disorder inherited as an autosomal recessive genetic trait.
    http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

    84. NORD - National Organization For Rare Disorders, Inc.
    Bardet Biedl syndrome. To purchase fulltext report ($7.50) Copyright 1994,1996, 2001, 2002 Synonyms of Bardet Biedl syndrome Biedl-Bardet syndrome.
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl

    85. Bardet Biedel Syndrome
    Hereditary Obesity Bardet Biedl syndrome. The Extra digits and obesityare two of the cardinal features of Bardet Biedl syndrome. In
    http://www.ophth.uiowa.edu/BBS.html
    Hereditary Obesity - Bardet Biedl Syndrome
    The Bardet Biedl syndrome is an autosomal recessive disorder characterized by obesity, retinal degeneration, extra digits on the hands and feet, and mental retardation. Just as identifying the genes for early-onset, hereditary forms of macular degeneration and glaucoma may provide clues to the more common late-onset forms of these diseases, we are hopeful that the identification of a gene for Bardet Biedl Syndrome will provide important insight into the common forms of pathological human obesity. Extra digits and obesity are two of the cardinal features of Bardet Biedl Syndrome. In late 1993, we mapped the first gene for Bardet Biedl syndrome to the long arm of chromosome 16 by studying a large inbred family from Israel. In 1994, we mapped two other genes for this disorder to chromosomes 3, and 15 in additional Bedouin families from Israel. We have also developed a new technique for gene mapping in inbred families that significantly reduces the time required to find the chromosomal location of a gene. We are currently applying this new method to a variety of different recessive diseases. Highly polymorphic genetic markers are used to identify the chromosomal location of disease-causing genes.

    86. Bardet – Biedl Syndrome
    one click … For Medical Professionals only. Bardet – biedl syndrome,,Print this article, (Georges Bardet, born 1885, French physician
    http://www.amershamhealth.com/medcyclopaedia/Volume VII/BARDET BIEDL SYNDROME.a
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    *For Medical Professionals only, registration required Bardet – biedl syndrome, (Georges Bardet, born 1885, French physician; Artur Biedl, 1869–1933, Austrian physician), this shares with Laurence Moon Biedl syndrome pigmented retinopathy, hypogonadism and renal tract abnormalities but also involves polydactyly. Inheritance is autosomal recessive. Radiology: polydactyly and urinary tract anomalies — cysts, and small or large echogenic kidneys.
    HC
    The Encyclopaedia of Medical Imaging Volume VII
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    This site is open to a public audience, still we want to know a little more about our visitors. Please tick off the boxes that match your profile.
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    87. Healthfinder® — Laurence Moon Bardet Biedl Syndrome Information And Referral S
    Links to support services, organizations, genetic societies, treatment clinics andother resources related to Laurence Moon Bardet Biedl syndrome.
    http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=4525&lang=1

    88. Health Library: All Topics: L: Laurence-Moon-Biedl Syndrome - Healthfinder®
    Laurence Moon Bardet Biedl syndrome Information and Referral Services Links to supportservices, organizations, genetic societies, treatment clinics and other
    http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=485

    89. Health Library - Laurence Moon Bardet Biedl Syndrome
    Your Health. Search. Laurence Moon Bardet Biedl syndrome. Self Help Clearinghouse.Laurence Moon Bardet Biedl syndrome. National network.
    http://yourhealth.stlukesonline.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=

    90. Health Library - Laurence Moon Bardet Biedl Syndrome
    Advanced Search. Laurence Moon Bardet Biedl syndrome. Self Help Clearinghouse.Laurence Moon Bardet Biedl syndrome. National network.
    http://www.stjudemedicalcenter.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=s

    91. Health Library - Bardet Biedl Syndrome
    Advanced Search. Bardet Biedl syndrome. None. General Discussion. BardetBiedlsyndrome is a rare disorder inherited as an autosomal recessive genetic trait.
    http://www.stjudemedicalcenter.org/library/healthguide/IllnessConditions/topic.a

    92. Health Library - Laurence Moon Bardet Biedl Syndrome
    SEARCH. Laurence Moon Bardet Biedl syndrome. Self Help Clearinghouse.Laurence Moon Bardet Biedl syndrome. National network.
    http://www.muskogeehealth.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29l

    93. Katalog - Wirtualna Polska
    Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce.
    http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Neurological_Disorders/
    Poczta Czat SMS Pomoc Szukaj.wp.pl: -Katalog -Polskie www -¦wiatowe www -Wirtualna Polska -FTP/Pliki -Grupy dyskusyjne -Encyklopedia -Produkty wp.pl Katalog Katalog ¦wiatowy DMOZ ... Neurological Disorders > Brain Diseases Fakty o Katalogu Pomoc Regulamin Serwis szukaj ... Ostatnio dodane
    NAWIGACJA Fakty o katalogu
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    94. Online And Offline Support: L
    Homepage address http//www.geocities.com/HotSprings/9308/. LaurenceMoon-Bardet-BiedlSyndrome. Please note Laurence-Moon-Bardet
    http://www.widesmiles.org/support/l.html
    L Langer-Giedion Syndrome Langer-Giedion Syndrome Association
    • People served: Individuals and families dealing with Langer-Giedion Syndrome Services provided: Information, public awareness, support for families, newsletter, and advocacy for research Contact people: Laurence-Moon-Bardet-Biedl Syndrome Please note: Laurence-Moon-Bardet-Biedl Syndrome includes specific facial characteristics that do not require reconstructive surgery. The LMBBS Society (United Kingdom)
      • People served: Families dealing with Laurence-Moon-Biedl Syndrome Services provided: Support and information Address: Spring Grove, Loudhams Wood Lane, Chalfont St Giles Bucks HP8 4AR Phone number: 01494 764924
      Laurence Moon Bardet Biedl Syndrome (United States)
      • People served: Families dealing with Laurence Moon Bardet Biedl Syndrome Services provided: Support and information Address: 124 Lincoln Avenue, Purchase NY 10577

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