Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects.
about
A case associated with comorbidities among cerebral infarction, idiopathic thrombocytopenic purpura, and triple x syndrome.Structural and numerical changes of chromosome X in patients with esophageal atresiaJejunal atresia in an infant with triple-X syndrome.Cross-sectional study shows that impaired bone mineral status and metabolism are found in nonmosaic triple X syndrome.Duodenal atresia in an infant with triple-X syndrome: A new associated malformation in 47,XXX
P2860
Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@en
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@nl
type
label
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@en
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@nl
prefLabel
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@en
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@nl
P2093
P356
P1476
Case report of a 22-week fetus ...... iple lower mesodermal defects.
@en
P2093
Schneider NR
Timmons CF
P2888
P356
10.1007/S100249900090
P577
1999-01-01T00:00:00Z