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T Attie-Bitach

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Human Mutation|April 3, 2007

Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.

Clinical Genetics|April 11, 2016

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangiaJ Thevenon, L Duplomb, S Phadke, et al.

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Search research articles

Showing results (11-20 of 12) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 12 results.

Human Mutation|April 3, 2007

Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.

Clinical Genetics|April 11, 2016

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangiaJ Thevenon, L Duplomb, S Phadke, et al.

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