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CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family by Mahdieh Daliri Ghouchanatigh, Ranjha Khan, Majid Mojarrad, Uzma Hameed, Muhammad Zubair, Ahmed Waqas, Mohsen Jalali, Mahmoudreza Kalantari, Ali Shamsa, Huan Zhang, Qing-Hua Shi
Published 2022-01-01
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A novel homozygous frameshift variant in DNAH8 causes multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family by Sobia Dil, Asad Khan, Ahsanullah Unar, Meng-Lei Yang, Imtiaz Ali, Aurang Zeb, Huan Zhang, Jian-Teng Zhou, Muhammad Zubair, Khalid Khan, Shun Bai, Qing-Hua Shi
Published 2023-01-01
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