McElhinney, D B <br/><br/>
Familial absent pulmonary valve syndrome without deletions of chromosome 22q11.  [electronic resource] 

 -  Cardiology in the young  Nov 2000 
 - 618-20 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1047-9511 
<br/><br/><label>Standard No.: </label>10.1017/s1047951100008908  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosomes, Human, Pair 22--genetics<br/>Family Health<br/>Female<br/>Gene Deletion<br/>Humans<br/>Infant<br/>Male<br/>Pulmonary Valve--abnormalities<br/>Tetralogy of Fallot--genetics