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

PRENATAL DIAGNOSIS (2017)

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PRENATAL DIAGNOSIS
Volume 37, Issue 10, Pages 1055-1056

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WILEY
DOI: 10.1002/pd.5137

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Genetics & Heredity Obstetrics & Gynecology

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