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Berrin Konuk
Berrin Konuk
Ankara University
Short stature
Genetics
Mutation
Exon
Sanger sequencing
2
Papers
174
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Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
2011
American Journal of Human Genetics
Asli Sirmaci
Michail Spiliopoulos
Francesco Brancati
Eric Powell
Duygu Duman
Alex Abrams
Guney Bademci
Emanuele Agolini
Shengru Guo
Berrin Konuk
Aslı Kavaz
Susan H. Blanton
Maria Christina Digilio
Bruno Dallapiccola
Juan Young
Stephan L Zuchner
Mustafa Tekin
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Citations (163)
A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy.
2007
Clinical Dysmorphology
T may Do anc
Berrin Konuk
Nursel Alpan
Onur Konuk
Riikka H. H m l inen
Anna-Elina Lehesjoki
Mustafa Tekin
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Citations (11)
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