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Archives of Ophthalmology (Chicago, Ill. : 1960)|March 26, 1998
Clinical features in affected individuals from 21 pedigrees with dominant optic atrophyM Votruba, F W Fitzke, G E Holder, et al.Human Mutation|March 29, 2000
Novel mutations of the RPGR gene in RP3 familiesI Zito, M B Gorin, C Plant, et al.European Psychiatry : the Journal of the Association of European Psychiatrists|May 26, 2017
The long-term association of OCD and depression and its moderators: A four-year follow up study in a large clinical sampleL Tibi, P van Oppen, A J L M van Balkom, et al.Genomics|October 1, 1992
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13)M E Porteous, A Curtis, S Lindsay, et al.Journal of Medical Genetics|June 1, 1996
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17pE E Tarttelin, C Plant, J Weissenbach, et al.European Journal of Human Genetics : EJHG|October 20, 2000
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophiesD A Bessant, A M Payne, C Plant, et al.Human Molecular Genetics|January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1pA C Ionides, V Berry, D S Mackay, et al.Current Eye Research|September 1, 1993
Confirmation of the rod cGMP phosphodiesterase beta subunit (PDE beta) nonsense mutation in affected rcd-1 Irish setters in the UK and development of a diagnostic testP J Clements, C Y Gregory, S M Peterson-Jones, et al.European Journal of Human Genetics : EJHG|January 1, 1994
A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28A R Curtis, S Lindsay, E Boye, et al.American Journal of Human Genetics|January 1, 1991
A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosaC F Inglehearn, R Bashir, D H Lester, et al.Pageof 18