Cavani, S <br/><br/>
Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations.  [electronic resource] 

 -  Prenatal diagnosis  Oct 2003 
 - 819-23 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.678  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adult<br/>Chromosomes, Human, Pair 1<br/>Chromosomes, Human, Pair 6<br/>Diagnosis, Differential<br/>Family<br/>Fatal Outcome<br/>Female<br/>Fetal Growth Retardation--complications<br/>Genetic Counseling<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Pedigree<br/>Pregnancy<br/>Pregnancy Trimester, Third<br/>Prenatal Diagnosis<br/>Telencephalon--abnormalities<br/>Translocation, Genetic