Search Results - Maryam Hassanlou

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    Prenatal diagnosis of citrullinemia type 1; seven families with c.1168G > A mutation of Argininosuccinate synthetase 1 gene in Southwest Iran: A case series by Maryam Hassanlou, Maryam Abiri, Sirous Zeinali

    Published 2022
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    An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype by Maryam Abiri, Maryam Hassanlou, Nima Narimani, Marzieh Zamani, Zahra Moeini

    Published 2021
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