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D M Hunt

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American Journal of Human Genetics|August 3, 2001

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophyS E Wilkie, Y Li, E C Deery, et al.

Molecular Cell|September 8, 2001

A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)E N Vithana, L Abu-Safieh, M J Allen, et al.

Ophthalmology|January 27, 2000

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.

Journal of Molecular Evolution|June 18, 1998

Molecular genetics of spectral tuning in New World monkey color visionS K Shyue, S Boissinot, H Schneider, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.

Pageof 19

Search research articles

Showing results (181-190 of 185) with videos related to

Sort By:

Pageof 19

You have reached the last page of results.This site can display upto 185 results.

American Journal of Human Genetics|August 3, 2001

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophyS E Wilkie, Y Li, E C Deery, et al.

Molecular Cell|September 8, 2001

A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)E N Vithana, L Abu-Safieh, M J Allen, et al.

Ophthalmology|January 27, 2000

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.

Journal of Molecular Evolution|June 18, 1998

Molecular genetics of spectral tuning in New World monkey color visionS K Shyue, S Boissinot, H Schneider, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.

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