Ma, Cong <br/><br/>
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.  [electronic resource] 

 -  BMC medical genetics  11 2019 
 - 169 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2350 
<br/><br/><label>Standard No.: </label>10.1186/s12881-019-0917-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Carrier Proteins--genetics<br/>Deafness--genetics<br/>Female<br/>Finger Joint--abnormalities<br/>Humans<br/>Joint Diseases--congenital<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Prenatal Diagnosis