about
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndromeThe molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.Chromosomal rearrangement as the basis for human tumourigenesis.Genome stability: What we have learned from cohesinopathies.Long-term survival after corrective surgeries in two patients with severe deformities due to Roberts syndrome: A Case report and review of the literature.
P2860
description
1988 nî lūn-bûn
@nan
1988 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Rhabdomyosarcoma in Roberts syndrome.
@ast
Rhabdomyosarcoma in Roberts syndrome.
@en
Rhabdomyosarcoma in Roberts syndrome.
@nl
type
label
Rhabdomyosarcoma in Roberts syndrome.
@ast
Rhabdomyosarcoma in Roberts syndrome.
@en
Rhabdomyosarcoma in Roberts syndrome.
@nl
prefLabel
Rhabdomyosarcoma in Roberts syndrome.
@ast
Rhabdomyosarcoma in Roberts syndrome.
@en
Rhabdomyosarcoma in Roberts syndrome.
@nl
P2093
P1476
Rhabdomyosarcoma in Roberts syndrome.
@en
P2093
Bellinger M
P304
P356
10.1016/0165-4608(88)90230-0
P577
1988-04-01T00:00:00Z