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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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W K Seltzer

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American Journal of Human Genetics|March 1, 1994

Genetic analysis of Hispanic individuals with cystic fibrosisT A Grebe, W K Seltzer, J DeMarchi, et al.

American Journal of Human Genetics|October 1, 1992

Mutation analysis of the cystic fibrosis transmembrane regulator gene in Native American populations of the southwestT A Grebe, W W Doane, S F Richter, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993

Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.

JAMA|November 17, 2001

A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic familiesE S Athan, J Williamson, A Ciappa, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

American Journal of Human Genetics|March 1, 1994

Genetic analysis of Hispanic individuals with cystic fibrosisT A Grebe, W K Seltzer, J DeMarchi, et al.

American Journal of Human Genetics|October 1, 1992

Mutation analysis of the cystic fibrosis transmembrane regulator gene in Native American populations of the southwestT A Grebe, W W Doane, S F Richter, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993

Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.

JAMA|November 17, 2001

A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic familiesE S Athan, J Williamson, A Ciappa, et al.

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