Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip.
about
Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2.Genome wide association study of Stayability and Heifer Pregnancy in Red Angus Cattle.A "Triple Trouble" Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy
P2860
Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip.
description
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name
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@ast
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@en
type
label
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@ast
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@en
prefLabel
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@ast
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@en
P2093
P2860
P1433
P1476
Exome sequencing identified ra ...... opmental dysplasia of the hip.
@en
P2093
Alia M Albalawi
Essa Alharby
Khalid I Khoshhal
P2860
P2888
P356
10.1186/S12881-017-0393-8
P50
P577
2017-03-21T00:00:00Z
P6179
1084250396