Gökhan Nalbant

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 2

Top Topics

Mitochondrial Dna

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Mine Koprulu, Muhammad Naeem, Gökhan Nalbant, Rana M Kamran Shabbir, Tariq Mahmood, Zele Huma, Sajid Malik, Aslıhan Tolun
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies. European journal of human genetics : EJHG 30 (11) (2022)
Sajid Malik, Gökhan Nalbant, Moqadsa Noreen, Muhammad Afzal, Aslıhan Tolun
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods. American journal of medical genetics. Part A (2021)