Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome-Reference-Cited by-同舟云学术

Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome

Published:2014-12 Issue:6 Volume:95 Page:763-770
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ehmke Nadja,Caliebe Almuth,Koenig Rainer,Kant Sarina G.,Stark Zornitza,Cormier-Daire Valérie,Wieczorek Dagmar,Gillessen-Kaesbach Gabriele,Hoff Kirstin,Kawalia Amit,Thiele Holger,Altmüller Janine,Fischer-Zirnsak Björn,Knaus Alexej,Zhu Na,Heinrich Verena,Huber Celine,Harabula Izabela,Spielmann Malte,Horn Denise,Kornak Uwe,Hecht Jochen,Krawitz Peter M.,Nürnberg Peter,Siebert Reiner,Manzke Hermann,Mundlos Stefan

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference55 articles.

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