Webb, A L <br/><br/>
Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation.  [electronic resource] 

 -  Prenatal diagnosis  Oct 1996 
 - 958-62 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1097-0223(199610)16:10<958::AID-PD971>3.0.CO;2-U  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amniocentesis--adverse effects<br/>Chorionic Villi Sampling--adverse effects<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 2<br/>Female<br/>Fetal Growth Retardation--genetics<br/>Fetal Membranes, Premature Rupture--diagnosis<br/>Fundoplication<br/>Gestational Age<br/>Hernia, Hiatal--surgery<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Maternal Age<br/>Mosaicism<br/>Placenta<br/>Pregnancy<br/>Pregnancy, High-Risk<br/>Pyloric Stenosis--congenital<br/>Renal Insufficiency--diagnosis<br/>Trisomy<br/>Ultrasonography, Prenatal