The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case-control study-Reference-Cited by-同舟云学术

The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case-control study

Published:2013-05-25 Issue:7 Volume:161 Page:1654-1661
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Armstrong Linlea¹,Jett Kimberly¹,Birch Patricia¹,Kendler David L.²,McKay Heather,Tsang Erica¹,Stevenson David A.³,Hanley David A.⁴,Egeli Deetria,Burrows Melonie,Friedman J.M.

Affiliation:

1. Department of Medical Genetics; University of British Columbia; Vancouver, BC; Canada

2. Department of Medicine (Endocrinology); University of British Columbia; Vancouver, BC; Canada

3. Division of Medical Genetics; University of Utah; Salt Lake City, Utah

4. Division of Endocrinology and Metabolism, Faculty of Medicine; Foothills Hospital and University of Calgary; Calgary, Alberta; Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference34 articles.

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3. Adolescents' self-assessment of sexual maturation;Duke;Pediatrics,1980

4. Decreased bone mineral density in neurofibromatosis type 1: Results from a pediatric cohort;Dulai;J Pediatr Orthop,2007

5. Bone metabolism markers and bone mineral density in children with neurofibromatosis type-1;Duman;Brain Dev,2008

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