Harvard Catalyst Profiles

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Bardet-Biedl Syndrome

"Bardet-Biedl Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8)


This graph shows the total number of publications written about "Bardet-Biedl Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Bardet-Biedl Syndrome" was a major or minor topic of these publication.
Bar chart showing 20 publications over 14 distinct years, with a maximum of 3 publications in 2014
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.