Liao, Jun <br/><br/>
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2012 
 - 1166-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.3977  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cells, Cultured<br/>Chorionic Villi Sampling<br/>Chromosome Deletion<br/>Chromosome Disorders--diagnosis<br/>Chromosome Fragile Sites--genetics<br/>Chromosomes, Human, Pair 10<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Mosaicism<br/>Phenotype<br/>Pregnancy<br/>Pregnancy Outcome--epidemiology<br/>Pregnancy Trimester, First--genetics<br/>Prenatal Diagnosis--methods<br/>Prevalence