Moradkhani, Kamran <br/><br/>
Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2006 
 - 1179-82 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.1585  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abortion, Induced<br/>Adult<br/>Amniocentesis<br/>Chorionic Gonadotropin, beta Subunit, Human--blood<br/>Chromosome Disorders--diagnosis<br/>Chromosomes, Human, Pair 16<br/>Female<br/>Fetal Diseases--diagnosis<br/>Fetal Growth Retardation--genetics<br/>Humans<br/>Karyotyping<br/>Male<br/>Mosaicism<br/>Phenotype<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Trisomy<br/>Ultrasonography<br/>alpha-Fetoproteins--analysis