학술논문
Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
Document Type
Article
Author
Jolly, A.; Du, H.; Grochowski, C.M.; Duan, R.; Fatih, J.M.; Dawood, M.; Van den Veyver, I.B.; Sutton, V.R.; Gibbs, R.A.; Wu, N.; Coban-Akdemir, Z.H.; Posey, J.E.; Lupski, J.R.; Borel, C.; Antonarakis, S.E.; Chen, N.; Zhu, L.; Zhao, S.; Salvi, S.; Jhangiani, S.N.; Muzny, D.M.; Koch, A.; Brucker, S.; Rouskas, K.; Glentis, S.; Dimas, A.S.; Deligeoroglou, E.; Bacopoulou, F.; Wise, C.A.; Dietrich, J.E.
Source
In: Human Genetics and Genomics Advances . (Human Genetics and Genomics Advances, 13 July 2023, 4(3))
Subject
Language
English
ISSN
26662477