Chuang, Louise <br/><br/>
Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations.  [electronic resource] 

 -  Prenatal diagnosis  Feb 2003 
 - 134-7 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.552  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Abortion, Eugenic<br/>Adult<br/>Chromosomes, Human, Pair 7<br/>Fathers<br/>Female<br/>Heredity--genetics<br/>Heterozygote<br/>Holoprosencephaly--diagnosis<br/>Humans<br/>Male<br/>Pregnancy<br/>Pregnancy Trimester, First<br/>Prenatal Diagnosis--methods<br/>Spectral Karyotyping<br/>Translocation, Genetic