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Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation

✍ Scribed by Ben Khelifa, Hela; Soyah, Najla; Ben-Abdallah-Bouhjar, Inesse; Gritly, Ryma; Sanlaville, Damien; Elghezal, Hatem; Saad, Ali; Mougou-Zerelli, Soumaya

Book ID: 121231777
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 981 KB
Volume: 527
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.06.018

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