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De novo variants in TCF7L2 are associated with a syndromic ..:

Dias, Caroline ; Pfundt, Rolph ; Kleefstra, Tjitske...
American Journal of Medical Genetics Part A. 185 (2021) 8 - p. 2384-2390 , 2021

Link: https://doi.org/10.1002/ajmg.a.62254

RT Journal
T1 <Title>De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder</Title>

UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.62254&Exemplar=1&LAN=DE
				
A1 Dias, Caroline
A1 Pfundt, Rolph
A1 Kleefstra, Tjitske
A1 Shuurs‐Hoeijmakers, Janneke
A1 Boon, Elles M. J.
A1 van Hagen, Johanna M.
A1 Zwijnenburg, Petra
A1 Weiss, Marjan M.
A1 Keren, Boris
A1 Mignot, Cyril
A1 Isapof, Arnaud
A1 Weiss, Karin
A1 Hershkovitz, Tova
A1 Iascone, Maria
A1 Maitz, Silvia
A1 Feichtinger, René G.
A1 Kotzot, Dieter
A1 Mayr, Johannes A.
A1 Ben‐Omran, Tawfeg
A1 Mahmoud, Laila
A1 Pais, Lynn S.
A1 Walsh, Christopher A.
A1 Shashi, Vandana
A1 Sullivan, Jennifer A.
A1 Stong, Nicholas
A1 Lecoquierre, Francois
A1 Guerrot, Anne‐Marie
A1 Charollais, Aude
A1 Rodan, Lance H.
PB Wiley
YR 2021
SN 1552-4825
SN 1552-4833
JF American Journal of Medical Genetics Part A
VO 185
IS 8
SP 2384
OP 2390
LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.62254
DO https://doi.org/10.1002/ajmg.a.62254
SF ELIB - SuUB Bremen

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