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)

Pedace, L (author)

de Boer, E (author)

Jackson, A (author)

Stellacci, E (author)

Lo Cicero, S (author)

Dentici, ML (author)

McWalter, K (author)

Sanchez-Lara, PA (author)

Lindstrom, K (author)

Madan-Khetarpal, S (author)

MacKenzie, JJ (author)

Monteleone, B (author)

Zhou, DH (author)

Sawyer, SL (author)

Monteiro, FP (author)

Macke, EL (author)

Iascone, M (author)

Selicorni, A (author)

Tenconi, R (author)

Amor, DJ (author)

Stals, K (author)

Cabet, S (author)

Steindl, K (author)

Weiss, K (author)

Castle, AMR (author)

Kalsner, L (author)

Chandler, KE (author)

Sheehan, W (author)

Shinde, DN (author)

Goodloe, D (author)

Bluske, K (author)

Faletra, F (author)

Kurtz-Nelson, EC (author)

Anderlid, BM (author)

Karolinska Institutet

Barakat, TS (author)

Graham, JM (author)

Faivre, L (author)

Banka, S (author)

Wang, TY (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)

2022

2022

English.

In: EUROPEAN JOURNAL OF HUMAN GENETICS. - 1018-4813. ; 30:SUPPL 1, s. 25-26

Related links:

http://kipublication...

• Conference paper (other academic/artistic)