Osteopathia striata with cranial sclerosis owing to WTX gene defect-Reference-Cited by-同舟云学术

Osteopathia striata with cranial sclerosis owing to WTX gene defect

Published:2009-12-18 Issue:1 Volume:25 Page:82-90
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Perdu Bram,Freitas Fenna de,Frints Suzanne GM,Schouten Meyke,Schrander-Stumpel Connie,Barbosa Mafalda,Pinto-Basto Jorge,Reis-Lima Margarida,Vernejoul Marie-Christine de,Becker Kristin,Freckmann Marie-Louise,Keymolen Kathlijn,Haan Eric,Savarirayan Ravi,Koenig Rainer,Zabel Bernhard,Vanhoenacker Filip M,Hul Wim Van

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Molecular genetics of too much bone;Janssens;Hum Mol Genet.,2002

2. L'image radiologique non encore décrite d'une anomalie du squelette;Voorhoeve;Acta Radiol.,1924

3. Osteopathia striata-Voorhoeve's disease: report of a case presenting the features of osteopathia striata and osteopetrosis;Hurt;J Bone Joint Surg.,1953

4. Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis;Jenkins;Nat Genet.,2009

5. Further clinical delineation and increased morbidity in males with osteopathia striata with cranial sclerosis: an X-linked disorder?;Pellegrino;Am J Med Genet.,1997

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