Associated Papers
Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.
Lemire G et al.
American Journal of Medical Genetics. Part A, 2021
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Fontana L et al.
Clinical Genetics, 2017
Analysis of WNT9B mutations in Chinese women with Mayer-Rokitansky-Küster-Hauser syndrome.
Wang M et al.
Reproductive Biomedicine Online, 2014
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