(Q37714586)

English

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

scientific article published on 10 March 2017

Statements

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU. (English)
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Christel Depienne
Caroline Nava
Boris Keren
Solveig Heide
Agnès Rastetter
Marie-Laure Moutard
Pankaj B Agrawal
Grace VanNoy
Joan M Stoler
Diane Doummar
Caroline Alby
Catherine Garel
Pauline Marzin
Sophie Scheidecker
Anne de Saint-Martin
Edouard Hirsch
Christian Korff
Armand Bottani
Christine Orzechowski
Lydie Burglen
Bruno Leheup
Joelle Roume
Chaitanya Datar
Michael J Parker
Laurent Pasquier
Sylvie Odent
Sophie Naudion
Marie-Ange Delrue
Bertrand Isidor
Florence Renaldo
Fiona Stewart
Udo Koehler
Birgit Häckl
Celina von Stülpnagel
Gerhard Kluger
Deb Pal
Tord Jonson
Maria Soller
Nienke E Verbeek
Mieke M van Haelst
Bobby Koeleman
Glen Monroe
Gijs van Haaften
DDD Study
Lucile Boutaud
Cyril Mignot
10 March 2017
136
463-479

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