Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal...

Clinical Case Reports 2018 / 08 Vol. 6; Iss. 8

Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH

Shariati, Gholamreza, Saberi, Alihossein, Hamid, Mohammad, Galehdari, Hamid, Sedaghat, Alireza, Abdorasuli, Nehzat
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Volume:
6
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.1604
Date:
August, 2018
File:
PDF, 463 KB
english, 2018
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