Microdeletion 5q14.3 and anomalies of brain development-Reference-Cited by-同舟云学术

Microdeletion 5q14.3 and anomalies of brain development

Published:2013-07-04 Issue:9 Volume:161 Page:2124-2133
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hotz Alrun¹,Hellenbroich Yorck²,Sperner Jürgen³,Linder-Lucht Michaela⁴,Tacke Uta⁴,Walter Caren¹,Caliebe Almuth⁵,Nagel Inga⁵,Saunders Dawn E.⁶,Wolff Gerhard¹,Martin Peter⁷,Morris-Rosendahl Deborah J.¹⁸

Affiliation:

1. Institute of Human Genetics; Albert-Ludwigs University Medical Centre Freiburg; Freiburg Germany

2. Institut für Humangenetik; Universität zu Lübeck; Lübeck Germany

3. Praxis für Neuropädiatrie; Lübeck Germany

4. Zentrum für Kinder- und Jugendmedizin; Albert-Ludwigs-Universitätsklinikum Freiburg; Freiburg Germany

5. Institut für Humangenetik; Christian-Albrechts-Universität Kiel; Kiel Germany

6. Department of Radiology; Great Ormond Street Hospital; London United Kingdom

7. Séguin Klinik; Epilepsiezentrum Kehl-Kork; Kork Germany

8. National Heart and Lung Institute; Imperial College, London; London United Kingdom

Funder

Dr. Heinrich-Kircher Foundation, Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36020/fullpdf

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5. Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum;Borozdin;J Med Genet,2004b

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