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American Journal of Human Genetics|September 6, 2001

CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.

European Journal of Human Genetics : EJHG|January 20, 2005

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsiaSusanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, et al.

Nature Genetics|January 29, 2013

Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesisStephen R F Twigg, Elena Vorgia, Simon J McGowan, et al.

Science (New York, N.Y.)|November 7, 2009

Genome sequence, comparative analysis, and population genetics of the domestic horseC M Wade, E Giulotto, S Sigurdsson, et al.

Pageof 48

Search research articles

Showing results (471-480 of 474) with videos related to

Sort By:

Pageof 48

You have reached the last page of results.This site can display upto 474 results.

American Journal of Human Genetics|September 6, 2001

CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.

European Journal of Human Genetics : EJHG|January 20, 2005

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsiaSusanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, et al.

Nature Genetics|January 29, 2013

Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesisStephen R F Twigg, Elena Vorgia, Simon J McGowan, et al.

Science (New York, N.Y.)|November 7, 2009

Genome sequence, comparative analysis, and population genetics of the domestic horseC M Wade, E Giulotto, S Sigurdsson, et al.

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