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S Bellman

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Human Molecular Genetics|November 5, 1997

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.

Clinical Genetics|September 5, 2001

Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 23 results.

Human Molecular Genetics|November 5, 1997

Clinical Genetics|September 5, 2001

Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

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