SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

Authors :: Radio, Francesca Clementina
Pang, Kaifang
Ciolfi, Andrea
Levy, Michael A.
Pedace, Lucia
Boer, Elke
Jackson, Adam
Stellacci, Emilia
Lo Cicero, Stefania
Dentici, Maria Lisa
Mcwalter, Kirsty
Sanchez-Lara, Pedro A.
Lindstrom, Kristin
Madan-Khetarpal, Suneeta
Mackenzie, Jennifer J.
Monteleone, Berrin
Zhou, Dihong
Sawyer, Sarah L.
Monteiro, Fabiola Paoli
Macke, Erica L.
Maria Iascone
Selicorni, Angelo
Tenconi, Romano
Amor, David J.
Stals, Karen
Cabet, Sara
Steindl, Katharina
Weiss, Karin
Castle, Alison M. R.
Kalsner, Louisa
Chandler, Kate E.
Sheehan, Willow
Shinde, Deepali N.
Goodloe, Dana
Bluske, Krista
Faletra, Flavio
Kurtz-Nelson, Evangeline C.
Anderlid, Britt-Marie
Barakat, Tahsin Stefan
Graham, John M.
Faivre, Laurence
Banka, Siddharth
Wang, Tianyun
Priolo, Manuela
Dallapiccola, Bruno
Vissers, Lisenka E. L. M.
Sadikovic, Bekim
Scott, Daryl A.
Holder, Jimmy Lloyd
Tartaglia, Marco
Source :: Web of Science

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