Lammer, E J <br/><br/>
Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?  [electronic resource] 

 -  Clinical dysmorphology  Jan 2001 
 - 9-13 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0962-8827 
<br/><br/><label>Standard No.: </label>10.1097/00019605-200101000-00002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Face--abnormalities<br/>Female<br/>Genes, Recessive<br/>Humans<br/>Hydrocephalus--diagnosis<br/>Infant<br/>Infant, Newborn<br/>Language Development Disorders--diagnosis<br/>Male<br/>Nuclear Family<br/>Pedigree<br/>Syndrome<br/>Tetralogy of Fallot--diagnosis