Van Opstal, D <br/><br/>
Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis.  [electronic resource] 

 -  Prenatal diagnosis  Sep 1993 
 - 825-32 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/pd.1970130906  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amniocentesis<br/>Chromosome Aberrations--diagnosis<br/>Chromosome Banding<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, Pair 18<br/>DNA Probes<br/>Dandy-Walker Syndrome--diagnosis<br/>Female<br/>Fetal Diseases--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence--methods<br/>Infant, Newborn<br/>Karyotyping<br/>Pregnancy<br/>Pregnancy Trimester, Second<br/>Pregnancy Trimester, Third<br/>Prenatal Diagnosis--methods<br/>Translocation, Genetic<br/>Trisomy