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                                       Details for article 18 of 23 found articles
 
 
  Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
 
 
Title: Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
Author: Jolly, Angad
Du, Haowei
Borel, Christelle
Chen, Na
Zhao, Sen
Grochowski, Christopher M.
Duan, Ruizhi
Fatih, Jawid M.
Dawood, Moez
Salvi, Sejal
Jhangiani, Shalini N.
Muzny, Donna M.
Koch, André
Rouskas, Konstantinos
Glentis, Stavros
Deligeoroglou, Efthymios
Bacopoulou, Flora
Wise, Carol A.
Dietrich, Jennifer E.
Van den Veyver, Ignatia B.
Dimas, Antigone S.
Brucker, Sara
Sutton, V. Reid
Gibbs, Richard A.
Antonarakis, Stylianos E.
Wu, Nan
Coban-Akdemir, Zeynep H.
Zhu, Lan
Posey, Jennifer E.
Lupski, James R.
Appeared in: Human genetics and genomics advances
Paging: Volume 4 () nr. 3 pages p.
Year: 2023
Contents:
Publisher: The Author(s)
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 18 of 23 found articles
 
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