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                                       Details for article 10 of 14 found articles
 
 
  Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions
 
 
Title: Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions
Author: Schönauer, Ria
Jin, Wenjun
Findeisen, Christin
Valenzuela, Irene
Devlin, Laura Alice
Murrell, Jill
Bedoukian, Emma C.
Pöschla, Linda
Hantmann, Elena
Riedhammer, Korbinian M.
Hoefele, Julia
Platzer, Konrad
Biemann, Ronald
Campeau, Philipp M.
Münch, Johannes
Heyne, Henrike
Hoffmann, Anne
Ghosh, Adhideb
Sun, Wenfei
Dong, Hua
Noé, Falko
Wolfrum, Christian
Woods, Emily
Parker, Michael J.
Neatu, Ruxandra
Le Guyader, Gwenael
Bruel, Ange-Line
Perrin, Laurence
Spiewak, Helena
Missotte, Isabelle
Fourgeaud, Melanie
Michaud, Vincent
Lacombe, Didier
Paolucci, Sarah A.
Buchan, Jillian G.
Glissmeyer, Margaret
Popp, Bernt
Blüher, Matthias
Sayer, John A.
Halbritter, Jan
Appeared in: The American journal of human genetics
Paging: Volume 110 () nr. 6 pages 998-1007
Year: 2023
Contents:
Publisher: American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 10 of 14 found articles
 
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