https://ck-1827452activator.co....m/grownup-jejuno-jej
While chromosome 1p36 deletion syndrome the most typical terminal subtelomeric microdeletion syndrome, 1p36 microduplications tend to be uncommon occasions. Polymicrogyria (PMG) is a brain malformation phenotype frequently contained in patients with 1p36 monosomy. The gene whose haploinsufficiency could cause this phenotype continues to be become identified. We used high-resolution arrayCGH in clients with various types o
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