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Phenotype and course of Hutchinson-Gilford progeria syndrome.
Merideth, Melissa A; Gordon, Leslie B; Clauss, Sarah; Sachdev, Vandana; Smith, Ann C M; Perry, Monique B; Brewer, Carmen C; Zalewski, Christopher; Kim, H Jeffrey; Solomon, Beth; Brooks, Brian P; Gerber, Lynn H; Turner, Maria L; Domingo, Demetrio L; Hart, Thomas C; Graf, Jennifer; Reynolds, James C; Gropman, Andrea; Yanovski, Jack A; Gerhard-Herman, Marie; Collins, Francis S; Nabel, Elizabeth G; Cannon, Richard O; Gahl, William A; Introne, Wendy J.
Affiliation
  • Merideth MA; National Human Genome Research Institute, Intramural Office of Rare Disease, National Institutes of Health, Bethesda, MD 20892-1851, USA.
N Engl J Med ; 358(6): 592-604, 2008 Feb 07.
Article in En | MEDLINE | ID: mdl-18256394
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Progeria Type of study: Guideline Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: N Engl J Med Year: 2008 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Progeria Type of study: Guideline Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: N Engl J Med Year: 2008 Type: Article Affiliation country: United States