Academic Journal
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
| العنوان: | SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females |
|---|---|
| المؤلفون: | Radio, FC, Ciolfi, A, Levy, MA, Pedace, L, de Boer, E, Stellacci, E, Lo Cicero, S, Dentici, ML, McWalter, K, Sanchez-Lara, PA, Lindstrom, K, Madan-Khetarpal, S, MacKenzie, JJ, Monteleone, B, Sawyer, SL, Monteiro, FP, Macke, EL, Iascone, M, Selicorni, A, Tenconi, R, Amor, DJ, Stals, K, Cabet, S, Steindl, K, Weiss, K, Castle, AMR, Kalsner, L, Sheehan, W, Shinde, DN, Goodloe, D, Bluske, K, Faletra, F, Kurtz-Nelson, EC, Anderlid, BM, Barakat, TS, Faivre, L, Banka, S, Priolo, M, Dallapiccola, B, Vissers, LELM, Sadikovic, B, Tartaglia, M |
| المصدر: | Radio , FC , Ciolfi , A , Levy , MA , Pedace , L , de Boer , E , Stellacci , E , Lo Cicero , S , Dentici , ML , McWalter , K , Sanchez-Lara , PA , Lindstrom , K , Madan-Khetarpal , S , MacKenzie , JJ , Monteleone , B , Sawyer , SL , Monteiro , FP , Macke , EL , Iascone , M , Selicorni , A , Tenconi , R , Amor , DJ , Stals , K , Cabet , S , Steindl , K , Weiss .... |
| سنة النشر: | 2022 |
| المجموعة: | The University of Manchester: Research Explorer - Publications |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| Relation: | https://research.manchester.ac.uk/en/publications/18bdfbee-030a-43e0-a315-75f4a2997bd9 |
| الاتاحة: | https://research.manchester.ac.uk/en/publications/18bdfbee-030a-43e0-a315-75f4a2997bd9 https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_starter&SrcAuth=WosAPI&KeyUT=WOS:000779367700073&DestLinkType=FullRecord&DestApp=WOS |
| Rights: | info:eu-repo/semantics/restrictedAccess |
| رقم الانضمام: | edsbas.AAD5D84A |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |