Ming, P M <br/><br/>
Cytogenetic variants in holoprosencephaly. Report of a case and review of the literature.  [electronic resource] 

 -  American journal of diseases of children (1960)  Aug 1976 
 - 864-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0002-922X 
<br/><br/><label>Standard No.: </label>10.1001/archpedi.1976.02120090074014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Autopsy<br/>Brain--pathology<br/>Chromosomes, Human, 13-15<br/>Face--abnormalities<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Myocardium--pathology<br/>Trisomy