TY  - GEN
AU  - Webb,A L
AU  - Sturgiss,S
AU  - Warwicker,P
AU  - Robson,S C
AU  - Goodship,J A
AU  - Wolstenholme,J
TI  - Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation
SN  - 0197-3851
PY  - 1997///0227
KW  - Adult
KW  - Amniocentesis
KW  - adverse effects
KW  - Chorionic Villi Sampling
KW  - Chromosome Aberrations
KW  - Chromosomes, Human, Pair 2
KW  - Female
KW  - Fetal Growth Retardation
KW  - genetics
KW  - Fetal Membranes, Premature Rupture
KW  - diagnosis
KW  - Fundoplication
KW  - Gestational Age
KW  - Hernia, Hiatal
KW  - surgery
KW  - Humans
KW  - Infant, Newborn
KW  - Karyotyping
KW  - Maternal Age
KW  - Mosaicism
KW  - Placenta
KW  - Pregnancy
KW  - Pregnancy, High-Risk
KW  - Pyloric Stenosis
KW  - congenital
KW  - Renal Insufficiency
KW  - Trisomy
KW  - Ultrasonography, Prenatal
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/(SICI)1097-0223(199610)16:10<958::AID-PD971>3.0.CO;2-U
ER  -