Category: Research

Month: 08 Aug 2012

Issue: not yet available

Research demonstrates Bardet-Biedl syndrome (BBS) genotype correlations with specific clinical pheno

Research conducted at the Berman-Gund Laboratory for the Study of Retinal Degenerations at Harvard Medical School has shown that phenotypic differences recorded in the clinical assessment of Bardet Biedl syndrome (BBS) patients may help guide genetic testing and counseling for BBS patients. Matching particular phenotypes to genetic information may provide clear clinical applicability in managing genetic testing and clinical care.

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by Dr. Gearóid Tuohy   Dear EURETINA Members,   A very warm welcome to the December 4th, 2017 edition of EURETINA’s web-based digital magazine, “EURETINA Brief”. EURETINA are delighted to continue our delivery of up-to-date summary briefs on a range of topics of interest to retinal clinicians, specialists and researchers across Europe. This resource is […]