https://www.selleckchem.com/pr....oducts/crenolanib-cp
The mother had a karyotype of 46,XX,der(15) t(Y;15)(q12;p13). At 39 weeks of gestation, a 3006-g healthy female baby was delivered with no phenotypic abnormality. During follow-up at age six months, she manifested normal physical and psychomotor development. Prenatal diagnosis of a 15p+variant should include a differential diagnosis of genomic imbalance and UPD 15, and aCGH and polymorphic DNA marker analyses are useful under such a circumstance. Prenatal diagnosis of a 15p+ variant should include a differential diagnosis o
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