Mutations in the retinal guanylate cyclase ( RETGC-1 ) gene in dominant cone–rod dystrophy

By Hunt D.M.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1179-1184

Oxford University Press

Access to resources Recommend Favorite

A Locus for Autosomal Dominant Posterior Polar Cataract on Chromosome 1p

By Ionides Alexander C. W.   Berry Vanita   Mackay Donna S.   Moore Anthony T.   Bhattacharya Shomi S.   Shiels Alan  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 47-51

Oxford University Press

Access to resources Recommend Favorite

Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone–rod dystrophy

By Wilkie Susan E.   Newbold RichardJ.  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3065-3073

Oxford University Press

Access to resources Recommend Favorite

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

By Kannabiran Chitra   Singh Hardeep   Jalali Subhadra  

Human Genetics, Vol. 131, Iss. 5, 2012-05 ,pp. : 717-723

Springer Publishing Company

Access to resources Recommend Favorite

Identification of a genetic locus for autosomal dominant disseminated superficial actinic porokeratosis on chromosome 1p31.3-p31.1

By Liu Ping  

Human Genetics, Vol. 123, Iss. 5, 2008-06 ,pp. : 507-513

Springer Publishing Company

Access to resources Recommend Favorite