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عمومی::
ریزحذف
"phenotype-first" approach led to the identification of many of the wellknown microdeletion syndromes (and of course such classic conditions as
due to microduplications and microdeletions detectable only on molecular
CHD7, was discovered due to two patients with an 8q12 microdeletion
polydactyly syndrome, having found a microdeletion on chromosome
whom microarray revealed a de novo microdeletion (774 kb; contained 47
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