A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing.
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A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing.
description
2017 nî lūn-bûn
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2017年の論文
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name
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@en
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@nl
type
label
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@en
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@nl
prefLabel
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@en
A rare ANOS1 variant in siblin ...... ied by whole exome sequencing.
@nl
P2093
P2860
P50
P356
P1433
P1476
A rare ANOS1 variant in siblin ...... fied by whole exome sequencing
@en
P2093
A J Griswold
R I Clavijo
P2860
P356
10.1111/ANDR.12432
P577
2017-12-06T00:00:00Z