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Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome
Kehrer, Christina, Hoischen, Alexander, Menkhaus, Ralf, Schwab, Eva, Müller, Andreas, Kim, Sarah, Kreiß, Martina, Weitensteiner, Valerie, Hilger, Alina, Berg, Christoph, Geipel, Anne, Reutter, Heiko,Year:
2016
Language:
english
Journal:
Prenatal Diagnosis
DOI:
10.1002/pd.4920
File:
PDF, 147 KB
english, 2016