Bardet–Biedl Syndrome - Wikipedia, The Free Encyclopedia The Bardet–Biedl syndrome is a ciliopathic human genetic disorder that produces many effects and affects many body systems. It is characterized principally by obesity http://en.wikipedia.org/wiki/Bardet-Biedl_syndrome
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Bardet-Biedl Syndrome GeneReviews NCBI Bookshelf GeneReviews designates a molecular genetic test as clinically available only if the test is listed in the GeneTests Laboratory Directory by either a US CLIAlicensed laboratory http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bbs
Laurence-Moon-Bardet-Biedl Syndrome Forum - FamilyConnect FamilyConnect, a site for parents of children with visual impairments, was created by AFB and NAPVI so that families could support each other, share stories and concerns, and find http://www.familyconnect.org/message_board_subjects.asp?FolderID=56
Bardet-Biedl Syndrome The Foundation Fighting Blindness is a publiclysupported charity raising money to fund research for macular degeneration, retinitis pigmentosa (RP), Usher syndrome, Stagardt http://www.blindness.org/index.php?view=article&catid=38:other-retinal-disea
Bardet-Biedl Syndrome (www.whonamedit.com) BardetBiedl syndrome A syndrome of obesity, mental retardation, polydactyly, retinitis pigmentosa with vision loss progressing to blindness, and hypogonadism. Also known as http://www.whonamedit.com/synd.cfm/3745.html
Bardet-Biedl Syndrome (BBS) What causes BardetBiedl syndrome? How is Bardet-Biedl treated? Bardet-Biedl syndrome is a rare genetic disorder that affects the brain and can cause multiple physical problems http://www.visionrx.com/library/enc/enc_bardetbiedl.asp
Bardet-Biedl Syndrome Evaluation To find a Test in the Athena Test Catalog, enter your search term in the box provided and click 'search.' http://www.athenadiagnostics.com/content/test-catalog/find-test/service-detail/q
Bardet-Biedl Syndrome - Genetics Home Reference BardetBiedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among members of the http://ghr.nlm.nih.gov/condition/bardet-biedl-syndrome
Bardet-Biedl Syndrome Proteins Shown To Run An Export Business A protein complex mutated in human disease removes excess signaling molecules to prevent them from damaging cilia, say researchers. http://www.sciencedaily.com/releases/2009/12/091228105909.htm
NORD Bardet Biedl Syndrome National Organization for Rare Disorders is dedicated to helping people with rare, orphan diseases. Rarediseases.org contains information on the prevention, treatment and cure of http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl
Bardet-biedl Syndrome Articles, Journals And Biomedical Literature bardetbiedl syndrome articles, journals and biomedical literature about bardet-biedl syndrome from novoseek, the free biomedical search engine http://www.novoseek.com/SearchAction.action?corpus=MEDLINE&criterion=1&q
Bardet Biedl Syndrome Important It is possible that the main title of the report Bardet Biedl Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s http://children.webmd.com/bardet-biedl-syndrome
BARDET-BIEDL SYNDROME; BBS - OMIM OMIM, Online Mendelian Inheritance in Man, a database of human genes and genetic disorders developed by staff at Johns Hopkins and hosted on the Web by NCBI. http://www.ncbi.nlm.nih.gov/omim/209900
Bardet-Biedl Syndrome Clinical features rodcone dystrophy; postaxial polydactyly; central obesity; mental retardation; hypogonadism; renal dysfunction http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=449
Bardet-Biedl Syndrome Symptoms, Diagnosis, Treatments And Causes BardetBiedl Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. http://www.wrongdiagnosis.com/b/bardet_biedl_syndrome/intro.htm
BBS1 Human Gene (Bardet-Biedl Syndrome 1) - Rat Genome Database BBS1 (BardetBiedl syndrome 1) Mutations in this gene have been observed in patients with the major form (type 1) of Bardet-Biedl syndrome. The encoded protein may play a role in http://rgd.mcw.edu/generalSearch/RgdSearch.jsp?quickSearch=1&searchKeyword=1
CIGNA - Bardet Biedl Syndrome Bardet Biedl Syndrome General Discussion. BardetBiedl syndrome is a rare, genetic multisystem disorder characterized primarily by deterioration of the cells that receive http://www.cigna.com/healthinfo/nord988.html
Bardet-Biedl Syndrome Doctor Patient UK BardetBiedl Syndrome - It is named after Georges Louis Bardet, a French physician (born 1885) and after Artur Biedl, a Hungarian pathologist and e http://www.patient.co.uk/showdoc/40001347/
The Foundation Fighting Blindness - Bardet Biedl Syndrome BardetBiedl syndrome is a rare, inherited disorder that causes a number of abnormalities in the way certain parts of the body function. The symptoms vary greatly, and may http://www.ffb.ca/eye_conditions/bardet_biedl.html