Article
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.
The Turkish journal of pediatrics - 1 Jan 2019
Gürsoy Semra, Kutbay Yaşar Bekir, Özdemir Taha Reşid, Hazan Filiz
Abstract excerpt
Gürsoy S, Kutbay YB, Özdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. Turk J Pediatr 2019; 61: 589-593. Chromosome 2q37 deletion syndrome is a rare chromosomal disorder which is characterized by mild-moderate intellectual disability, brachymetaphalangy of digits 3-5, short stature, obesity, hypotonia and characteristic facial...
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