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Rare variant enrichment analysis supports GREB1L as a contr..:
Jolly, Angad
;
Du, Haowei
;
Borel, Christelle
...
Human Genetics and Genomics Advances. 4 (2023) 3 - p. 100188 , 2023
Link:
https://doi.org/10.1016/j.xhgg.2023.100188
RT Journal T1
Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.xhgg.2023.100188&Exemplar=1&LAN=DE A1 Jolly, Angad A1 Du, Haowei A1 Borel, Christelle A1 Chen, Na A1 Zhao, Sen A1 Grochowski, Christopher M. A1 Duan, Ruizhi A1 Fatih, Jawid M. A1 Dawood, Moez A1 Salvi, Sejal A1 Jhangiani, Shalini N. A1 Muzny, Donna M. A1 Koch, André A1 Rouskas, Konstantinos A1 Glentis, Stavros A1 Deligeoroglou, Efthymios A1 Bacopoulou, Flora A1 Wise, Carol A. A1 Dietrich, Jennifer E. A1 Van den Veyver, Ignatia B. A1 Dimas, Antigone S. A1 Brucker, Sara A1 Sutton, V. Reid A1 Gibbs, Richard A. A1 Antonarakis, Stylianos E. A1 Wu, Nan A1 Coban-Akdemir, Zeynep H. A1 Zhu, Lan A1 Posey, Jennifer E. A1 Lupski, James R. PB Elsevier BV YR 2023 SN 2666-2477 JF Human Genetics and Genomics Advances VO 4 IS 3 SP 100188 LK http://dx.doi.org/https://doi.org/10.1016/j.xhgg.2023.100188 DO https://doi.org/10.1016/j.xhgg.2023.100188 SF ELIB - SuUB Bremen
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