Hasil Pencarian - Mehdi Agha Gholizadeh
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A female with 46,XY Disorder of Sexual Development with normal SRY gene sequence: A case report oleh Mehdi Agha Gholizadeh, Afsaneh Bazgir, Faezeh Sarvar, Zahra Pakzad
Diterbitkan 2019-03-01
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Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the... oleh Mehdi Agha Gholizadeh, Mina Mohammadi-Sarband, Fatemeh Fardanesh, Masoud Garshasbi
Diterbitkan 2022-04-01
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