Hennekam, Raoul C M <br/><br/>
Hutchinson-Gilford progeria syndrome: review of the phenotype.  [electronic resource] 

 -  American journal of medical genetics. Part A  Dec 2006 
 - 2603-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31346  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Cardiovascular Diseases--pathology<br/>Child<br/>Female<br/>Humans<br/>Infant<br/>Lamin Type A--genetics<br/>Male<br/>Models, Genetic<br/>Mutation<br/>Osteolysis--pathology<br/>Phenotype<br/>Progeria--diagnosis