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Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia
Ben-Abdallah-Bouhjar, Inesse, Hannachi, Hanene, Labalme, Audrey, Gmidène, Abir, Mougou, Soumaya, Soyah, Najla, Gribaa, Moez, Sanlaville, Damien, Elghezal, Hatem, Saad, AliVolume:
55
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2012.04.011
Date:
August, 2012
File:
PDF, 469 KB
english, 2012