Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.
about
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarrayPerinatal Case of Fatal Simpson-Golabi-Behmel Syndrome with Hyperplasia of Seminiferous Tubules.Comment on "Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome".
P2860
Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
@wuu
2016年学术文章
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2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
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name
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@en
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@nl
type
label
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@en
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@nl
prefLabel
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@en
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@nl
P2093
P2860
P356
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P1476
Whole exome sequencing and arr ...... impson-Golabi-Behmel syndrome.
@en
P2093
Alina Hilger
Andreas Müller
Anne Geipel
Christina Kehrer
Christoph Berg
Eva Schwab
Heiko Reutter
Martina Kreiß
Ralf Menkhaus
P2860
P304
P356
10.1002/PD.4920
P577
2016-09-27T00:00:00Z