Meshcheryakova, Tatiana I <br/><br/>
A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.  [electronic resource] 

 -  Annals of human genetics  Mar 2015 
 - 148-52 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1469-1809 
<br/><br/><label>Standard No.: </label>10.1111/ahg.12098  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Branchio-Oto-Renal Syndrome--genetics<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation, Missense<br/>Russia<br/>Transcription Factor AP-2<br/>Young Adult