Reed, T <br/><br/>
Hypothesis: association of the critical region of trisomy 18 and 18q2--syndrome with dermatoglyphic findings and a growth suppressor (deleted in colon cancer) locus.  [electronic resource] 

 -  Clinical genetics  May 1991 
 - 391-5 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1991.tb03048.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Transformation, Neoplastic--genetics<br/>Chromosome Aberrations--genetics<br/>Chromosome Deletion<br/>Chromosome Disorders<br/>Colorectal Neoplasms--genetics<br/>DNA Probes<br/>Dermatoglyphics<br/>Gene Expression Regulation, Neoplastic--physiology<br/>Genes, Dominant--genetics<br/>Genes, Tumor Suppressor--genetics<br/>Genetic Linkage--genetics<br/>Humans<br/>Trisomy