Stene, J <br/><br/>
Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981.  [electronic resource] 

 -  Prenatal diagnosis  1984 
 - 81-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/pd.1970040707  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amniocentesis<br/>Chromosome Aberrations--diagnosis<br/>Chromosome Disorders<br/>Down Syndrome--diagnosis<br/>Europe<br/>Female<br/>Humans<br/>Karyotyping<br/>Male<br/>Maternal Age<br/>Mosaicism<br/>Paternal Age<br/>Pregnancy<br/>Recurrence<br/>Risk<br/>Sex Chromosome Aberrations--diagnosis<br/>Translocation, Genetic