Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia-Reference-Cited by-同舟云学术

Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia

Author:

Bergwitz C.¹²,Prochnau A.¹,Mayr B.¹,Kramer F.-J.³,Rittierodt M.⁴,Berten H.-L.⁵,Hausamen J.-E.³,Brabant G.¹

Affiliation:

1. Abteilung fü; r Klinische Endokrinologie; Hochschule Hannover Hannover Germany

2. ; Department of Medicine; Massachusetts General Hospital; Blossom St. Boston MA 02114 USA

3. Klinik und Poliklinik fü; r Mund-, Kiefer- und Gesichtschirurgie; Hochschule Hannover Hannover Germany

4. Klinik fü; r Neurochirurgie; Hochschule Hannover Hannover Germany

5. Klinik fü; r Kieferorthopädie der Medizinische; Hochschule Hannover Hannover Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference28 articles.

1. Bone mineral density in children and adolescents: relation to puberty, calcium intake, and physical activity;Boot;J Clin Endocrinol Metab,1997

4. A gene for cleidocraniel dysplasia maps to the short arm of chromosome 6;Feldman;Am J Hum Genet,1995

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