HomozygousHOXB1loss-of-function mutation in a large family with hereditary congenital facial paresis-Reference-Cited by-同舟云学术

HomozygousHOXB1loss-of-function mutation in a large family with hereditary congenital facial paresis

Published:2016-05-04 Issue:7 Volume:170 Page:1813-1819
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Vogel Markus¹,Velleuer Eunike²,Schmidt-Jiménez Leon F.³,Mayatepek Ertan¹,Borkhardt Arndt²,Alawi Malik⁴⁵⁶,Kutsche Kerstin³,Kortüm Fanny³

Affiliation:

1. Department of General Pediatrics; Neonatology and Pediatric Cardiology; University Children's Hospital; Heinrich-Heine University; Düsseldorf Germany

2. Department of Pediatric Oncology; Hematology and Clinical Immunology; University Children's Hospital; Heinrich Heine University; Düsseldorf Germany

3. Institute of Human Genetics; University Medical Center Hamburg-Eppendorf; Hamburg Germany

4. University Medical Center Hamburg-Eppendorf; Bioinformatics Service Facility; Hamburg Germany

5. Center for Bioinformatics; University of Hamburg; Hamburg Germany

6. Heinrich-Pette-Institute; Leibniz-Institute for Experimental Virology; Virus Genomics Hamburg Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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