Sung, Pi-Lin <br/><br/>
Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.  [electronic resource] 

 -  Taiwanese journal of obstetrics & gynecology  Jun 2012 
 - 260-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1875-6263 
<br/><br/><label>Standard No.: </label>10.1016/j.tjog.2012.04.017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Abortion, Induced<br/>Adult<br/>Agenesis of Corpus Callosum--diagnostic imaging<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 16<br/>Chromosomes, Human, Pair 2<br/>Chromosomes, Human, Pair 7<br/>Comparative Genomic Hybridization<br/>Female<br/>Humans<br/>Hydrocephalus--diagnostic imaging<br/>Karyotype<br/>Polydactyly--diagnostic imaging<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Trisomy<br/>Ultrasonography