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

Radio, FC (author)

Pang, KF (author)

Ciolfi, A (author)

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Levy, MA (author)

Hernandez-Garcia, A (author)

Pedace, L (author)

Pantaleoni, F (author)

Liu, ZD (author)

de Boer, E (author)

Jackson, A (author)

Bruselles, A (author)

McConkey, H (author)

Stellacci, E (author)

Lo Cicero, S (author)

Motta, M (author)

Carrozzo, R (author)

Dentici, ML (author)

McWalter, K (author)

Desai, M (author)

Monaghan, KG (author)

Telegrafi, A (author)

Philippe, C (author)

Vitobello, A (author)

Au, M (author)

Grand, K (author)

Sanchez-Lara, PA (author)

Baez, J (author)

Lindstrom, K (author)

Kulch, P (author)

Sebastian, J (author)

Madan-Khetarpal, S (author)

Roadhouse, C (author)

MacKenzie, JJ (author)

Monteleone, B (author)

Saunders, CJ (author)

Cuevas, JKJ (author)

Cross, L (author)

Zhou, DH (author)

Hartley, T (author)

Sawyer, SL (author)

Monteiro, FP (author)

Secches, TV (author)

Kok, F (author)

Schultz-Rogers, LE (author)

Macke, EL (author)

Morava, E (author)

Klee, EW (author)

Kemppainen, J (author)

Iascone, M (author)

Selicorni, A (author)

Tenconi, R (author)

Amor, DJ (author)

Pais, L (author)

Gallacher, L (author)

Turnpenny, PD (author)

Stals, K (author)

Ellard, S (author)

Cabet, S (author)

Lesca, G (author)

Pascal, J (author)

Steindl, K (author)

Ravid, S (author)

Weiss, K (author)

Castle, AMR (author)

Carter, MT (author)

Kalsner, L (author)

de Vries, BBA (author)

van Bon, BW (author)

Wevers, MR (author)

Pfundt, R (author)

Stegmann, APA (author)

Kerr, B (author)

Kingston, HM (author)

Chandler, KE (author)

Sheehan, W (author)

Elias, AF (author)

Shinde, DN (author)

Towne, MC (author)

Robin, NH (author)

Goodloe, D (author)

Vanderver, A (author)

Sherbini, O (author)

Bluske, K (author)

Hagelstrom, RT (author)

Zanus, C (author)

Faletra, F (author)

Musante, L (author)

Kurtz-Nelson, EC (author)

Earl, RK (author)

Anderlid, BM (author)

Karolinska Institutet

Morin, G (author)

van Slegtenhorst, M (author)

Diderich, KEM (author)

Brooks, AS (author)

Gribnau, J (author)

Boers, RG (author)

Finestra, TR (author)

Carter, LB (author)

Rauch, A (author)

Gasparini, P (author)

Boycott, KM (author)

Barakat, TS (author)

Graham, JM (author)

Faivre, L (author)

Banka, S (author)

Wang, TY (author)

Eichler, EE (author)

Priolo, M (author)

Dallapiccola, B (author)

Vissers, LELM (author)

Sadikovic, B (author)

Scott, DA (author)

Holder, JL (author)

Tartaglia, M (author)

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 (creator_code:org_t)

Elsevier BV, 2021

2021

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 108:3, s. 502-516

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• Journal article (peer-reviewed)