C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome-Reference-Cited by-同舟云学术

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C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome

Published:2011-03-04 Issue:6 Volume:48 Page:390-395
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Arts H. H.,Bongers E. M. H. F.,Mans D. A.,van Beersum S. E. C.,Oud M. M.,Bolat E.,Spruijt L.,Cornelissen E. A. M.,Schuurs-Hoeijmakers J. H. M.,de Leeuw N.,Cormier-Daire V.,Brunner H. G.,Knoers N. V. A. M.,Roepman R.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

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