Gershoni, Moran <br/><br/>
A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics  09 2017 
 - 998-1006 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-0366 
<br/><br/><label>Standard No.: </label>10.1038/gim.2016.225  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Azoospermia--diagnosis<br/>Biomarkers<br/>Biopsy<br/>Case-Control Studies<br/>Consanguinity<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Dyneins--genetics<br/>Family<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Genetic Testing<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Mutation<br/>Pedigree<br/>Spermatozoa--metabolism