Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype
about
Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and miceTelomeres: a diagnosis at the end of the chromosomesProspective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4A genome-wide scan for genes involved in primary vesicoureteric reflux.
P2860
Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Familial cryptic translocation ...... osteodystrophy-like phenotype
@ast
Familial cryptic translocation ...... osteodystrophy-like phenotype
@en
type
label
Familial cryptic translocation ...... osteodystrophy-like phenotype
@ast
Familial cryptic translocation ...... osteodystrophy-like phenotype
@en
prefLabel
Familial cryptic translocation ...... osteodystrophy-like phenotype
@ast
Familial cryptic translocation ...... osteodystrophy-like phenotype
@en
P2093
P2860
P1476
Familial cryptic translocation ...... osteodystrophy-like phenotype
@en
P2093
Bijlsma EK
Hennekam RC
Hoovers JM
Oude Luttikhuis ME
Sluitjer S
P2860
P304
P407
P577
1999-08-01T00:00:00Z