Gökhan Nalbant
2PUBLICATIONS
7CO-AUTHORS
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Publications (2)
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|Jun 08, 2022
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies.Mine Koprulu, Muhammad Naeem, Gökhan Nalbant
|Sep 27, 2021
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods.Sajid Malik, Gökhan Nalbant, Moqadsa Noreen
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