Gemmill, R M <br/><br/>
A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.  [electronic resource] 

 -  Genomics  Sep 1991 
 - 93-102 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1016/0888-7543(91)90105-n  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Line<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 3<br/>Electrophoresis, Gel, Pulsed-Field<br/>Facial Bones--abnormalities<br/>Genetic Linkage<br/>Humans<br/>Skull--abnormalities<br/>Syndactyly--genetics<br/>Syndrome<br/>Translocation, Genetic