Cusano, R <br/><br/>
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13.  [electronic resource] 

 -  European journal of human genetics : EJHG  Nov 2000 
 - 895-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1038/sj.ejhg.5200533  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 22--genetics<br/>DNA--genetics<br/>Eye Abnormalities<br/>Family Health<br/>Female<br/>Genotype<br/>Haplotypes<br/>Hearing Loss, Sensorineural<br/>Humans<br/>Italy<br/>Male<br/>Microsatellite Repeats<br/>Middle Aged<br/>Nephritis<br/>Pedigree<br/>Syndrome<br/>Thrombocytopenia