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J Vigneron

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Nature Genetics|February 1, 1997

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.

Nature Genetics|October 3, 1999

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.

Clinical Genetics|March 19, 2010

Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.

Human Mutation|November 7, 2009

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 44 results.

Nature Genetics|February 1, 1997

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.

Nature Genetics|October 3, 1999

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.

Clinical Genetics|March 19, 2010

Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.

Human Mutation|November 7, 2009

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.

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