Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families-Reference-Cited by-同舟云学术

Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families

Published:2017-03 Issue:3 Volume:60 Page:163-168
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Dinçsoy Bir Firdevs,Dinçkan Nuriye,Güven Yeliz,Baş Firdevs,Altunoğlu Umut,Kuvvetli Senem S.,Poyrazoğlu Şükran,Toksoy Güven,Kayserili Hülya,Uyguner Z. Oya

Funder

Scientific and Technological Research Institution of Turkey, TUBİTAK-ERA NET

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference32 articles.

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3. New approaches for interpreting projected bone densitometry data;Carter;J. bone mineral Res.,1992

4. A natural history of cleidocranial dysplasia;Cooper;Am. J. Med. Genet.,2001

5. Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2;El-Gharbawy;Am. J. Med. Genet. Part A,2010

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