Comment on “Whole exome sequencing and array-based...

Prenatal Diagnosis 2017 / 10 Vol. 37; Iss. 10

Comment on “Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome”

Fauth, Christine, Toutain, Annick
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Volume:
37
Language:
english
Journal:
Prenatal Diagnosis
DOI:
10.1002/pd.5137
Date:
October, 2017
File:
PDF, 66 KB
english, 2017
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