1q42.12q42.2 Deletion in a Child with Midline Defects and Hypoplasia of the Corpus Callosum

Devi, ARR; Ganapathy, A; Mannan, AU; Sabharanjak, S; Naushad, SM

Devi, ARR (reprint author), Rainbow Childrens Hosp, 2 Banjara Hills, Hyderabad 500034, India.

MOLECULAR SYNDROMOLOGY, 2019; 10 (3): 161

Abstract

Chromosome 1q42.12q42.2 deletions are documented as "disease causing" and show overlapping phenotypes depending on the genes involved in the deletion.......

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