Lee, C <br/><br/>
Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.  [electronic resource] 

 -  American journal of medical genetics  May 2001 
 - 246-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/1096-8628(20010501)100:3<246::aid-ajmg1254>3.0.co;2-n  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adult<br/>Cerebral Ventricles--abnormalities<br/>Chromosomes, Human, Pair 14<br/>Chromosomes, Human, Pair 21<br/>Cleft Palate--diagnostic imaging<br/>Cytogenetic Analysis<br/>Female<br/>Fetal Growth Retardation--diagnostic imaging<br/>Fetus--abnormalities<br/>Humans<br/>In Situ Hybridization, Fluorescence--methods<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Monosomy<br/>Pregnancy<br/>Pregnancy Trimester, Second<br/>Translocation, Genetic<br/>Trisomy<br/>Ultrasonography, Prenatal