Lantieri, F <br/><br/>
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.  [electronic resource] 

 -  Annals of human genetics  Jan 2006 
 - 12-26 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-4800 
<br/><br/><label>Standard No.: </label>10.1111/j.1529-8817.2005.00196.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Case-Control Studies<br/>DNA Mutational Analysis<br/>DNA Primers<br/>Evolution, Molecular<br/>Gene Components<br/>Genotype<br/>Haplotypes--genetics<br/>Hirschsprung Disease--genetics<br/>Humans<br/>Italy<br/>Linkage Disequilibrium<br/>Microsatellite Repeats--genetics<br/>Molecular Sequence Data<br/>Proto-Oncogene Mas<br/>Proto-Oncogene Proteins c-ret--genetics<br/>Recombination, Genetic--genetics<br/>Sequence Analysis, DNA