van Asperen, C J <br/><br/>
Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.  [electronic resource] 

 -  Journal of medical genetics  Apr 1998 
 - 323-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.35.4.323  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Genetic Diseases, Inborn<br/>Growth Disorders--complications<br/>Humans<br/>Male<br/>Neurofibromatosis 1--complications<br/>Syndrome