Microduplications upstream ofMSX2are associated with a phenocopy of cleidocranial dysplasia-Reference-Cited by-同舟云学术

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Microduplications upstream ofMSX2are associated with a phenocopy of cleidocranial dysplasia

Published:2012-06-20 Issue:7 Volume:49 Page:437-441
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Ott Claus Eric,Hein Hendrikje,Lohan Silke,Hoogeboom Jeannette,Foulds Nicola,Grünhagen Johannes,Stricker Sigmar,Villavicencio-Lorini Pablo,Klopocki Eva,Mundlos Stefan

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation;Frontiers in Genetics;2021-10-19

2. Genetic Disorders of Pituitary Development in Patients with Sheehan'S Syndrome;Acta Endocrinologica (Bucharest);2016

3. Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders;Briefings in Functional Genomics;2015-05-13

4. Deletions of chromosomal regulatory boundaries are associated with congenital disease;Genome Biology;2014-09

5. Leri’s pleonosteosis, a congenital rheumatic disease, results from microduplication at 8q22.1 encompassing GDF6 and SDC2 and provides insight into systemic sclerosis pathogenesis;Annals of the Rheumatic Diseases;2014-01-17

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