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Mutations in ANKRD11 Cause KBG Syndrome, Characterized by... | ResearchHub
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Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
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Authors
Aslı Sırmacı
16 more
Aslı Sırmacı
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Michail Spiliopoulos
14 more
•
Mustafa Tekin
Published
July 25, 2011
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Journal
The American Journal of Human Genetics
Topics
Biology
Dermatology
Medicine
Genetics
Molecular Biology
Show all topics
DOI
10.1016/j.ajhg.2011.06.007
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publisher-specific-oa
Supporters
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Journal
The American Journal of Human Genetics
Topics
Biology
Dermatology
Medicine
Genetics
Molecular Biology
Show all topics
DOI
10.1016/j.ajhg.2011.06.007
License
publisher-specific-oa
