Autosomal dominant brachyolmia in a large Swedish family: Phenotypic spectrum and natural course-Reference-Cited by-同舟云学术

Autosomal dominant brachyolmia in a large Swedish family: Phenotypic spectrum and natural course

Published:2014-03-26 Issue:7 Volume:164 Page:1635-1641
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Grigelioniene Giedre¹²³,Geiberger Stefan⁴,Horemuzova Eva⁵⁶,Moström Eva⁵⁷,Jäntti Nina¹²,Neumeyer Lo³,Åström Eva⁵⁸,Nordenskjöld Magnus¹²³,Nordgren Ann¹²³,Mäkitie Outi¹²³⁹

Affiliation:

1. Department of Molecular Medicine and Surgery; Karolinska Institutet; Stockholm Sweden

2. Center for Molecular Medicine; Karolinska Institutet; Stockholm Sweden

3. Department of Clinical Genetics; Karolinska University Hospital; Stockholm Sweden

4. Department of Pediatric Radiology; Karolinska University Hospital; Stockholm Sweden

5. Department for Women's and Children's Health; Karolinska Institutet; Stockholm Sweden

6. Paediatric Endocrinology Unit; Karolinska University Hospital; Stockholm Sweden

7. Department of Musculoskeletal Diseases and Advanced Home Care; Karolinska University Hospital; Stockholm Sweden

8. Department of Neuropediatrics; Karolinska University Hospital; Stockholm Sweden

9. Folkhälsan Institute of Genetics; Helsinki Finland

Funder

Sabbatical Leave Programme of the European Society for Paediatric Endocrinology

Eli Lilly International Corporation, the Folkhälsan Research Foundation and the Academy of Finland. Sunnerdahls and Norbacka-Eugenia Foundations

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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