Kantaputra, Piranit N <br/><br/>
Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion.  [electronic resource] 

 -  American journal of medical genetics. Part A  Dec 2006 
 - 2598-602 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31386  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 18<br/>Holoprosencephaly--diagnosis<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Hypotrichosis--diagnosis<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Microcephaly--genetics<br/>Phenotype<br/>Repressor Proteins--genetics<br/>Syndrome