Stewart, H <br/><br/>
Congenital disseminated neurofibromatosis type 1: a clinical and molecular case report.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2008 
 - 1444-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32305  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosomes, Human, Pair 17--genetics<br/>Female<br/>Genes, Neurofibromatosis 1<br/>Genes, p53<br/>Genetic Markers<br/>Germ-Line Mutation<br/>Humans<br/>Infant, Newborn<br/>Loss of Heterozygosity<br/>Neurofibromatosis 1--etiology<br/>Sequence Deletion