Hertz, J M <br/><br/>
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication.  [electronic resource] 

 -  Clinical genetics  Oct 1994 
 - 291-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1994.tb04162.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Charcot-Marie-Tooth Disease--genetics<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 17<br/>DNA Mutational Analysis<br/>Fathers<br/>Genomic Imprinting<br/>Humans<br/>Male<br/>Pedigree<br/>Repetitive Sequences, Nucleic Acid