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Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.Gene|November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)N B Haider, C Searby, E Galperin, et al.Cell Reports|December 18, 2015
Differential DNA Methylation Analysis without a Reference GenomeJohanna Klughammer, Paul Datlinger, Dieter Printz, et al.Plos One|April 4, 2014
Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse modelKhristofor Agassandian, Milan Patel, Marianna Agassandian, et al.Health Affairs (Project Hope)|March 3, 2025
The Indian Health Service Is Associated With Higher-Quality Perinatal Care For American Indian And Alaska Native PeopleJulia D Interrante, Jessica L Liddell, Emily C Sheffield, et al.Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, et al.Human Molecular Genetics|January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15R Carmi, T Rokhlina, A E Kwitek-Black, et al.American Journal of Medical Genetics. Part A|February 4, 2005
Ocular phenotypes of three genetic variants of Bardet-Biedl syndromeElise Héon, Carol Westall, Rivka Carmi, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Complement factor H polymorphism p.Tyr402His and cuticular DrusenMichael A Grassi, James C Folk, Todd E Scheetz, et al.Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.Pageof 41