Published in
Wiley, The American Journal of Medical Genetics - Part A, 8(185), p. 2384-2390, 2021
DOI: 10.1002/ajmg.a.62254
Links
Tools
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder
Journal article published in 2021 by
Caroline Dias 
,
Rolph Pfundt,
Tjitske Kleefstra,
Johanna M. van Hagen,
Janneke Shuurs‐Hoeijmakers,
Elles M. J. Boon,
Johanna M. Hagen,
Petra Zwijnenburg,
Marjan M. Weiss,
Boris Keren,
Cyril Mignot,
Arnaud Isapof,
Karin Weiss,
Tova Hershkovitz,
Maria Iascone
and other authors.
,
Rolph Pfundt,
Tjitske Kleefstra,
Johanna M. van Hagen,
Janneke Shuurs‐Hoeijmakers,
Elles M. J. Boon,
Johanna M. Hagen,
Petra Zwijnenburg,
Marjan M. Weiss,
Boris Keren,
Cyril Mignot,
Arnaud Isapof,
Karin Weiss,
Tova Hershkovitz,
Maria Iascone
and other authors.
This paper is made freely available by the publisher.
Full text: Download
Published version:
archiving forbidden
Data provided by 