Atypical progeroid syndrome: an unknown helicase gene defect?

Ruijs, M W G; van Andel, R N J; Oshima, J; Madan, K; Nieuwint, A W M; Aalfs, C M

Ruijs, M W G; van Andel, R N J; Oshima, J; Madan, K; Nieuwint, A W M; Aalfs, C M.

Affiliation

Ruijs MW; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.

Am J Med Genet A ; 116A(3): 295-9, 2003 Jan 30.

Article in En | MEDLINE | ID: mdl-12503110

Subject(s)

Progeria/genetics; Progeria/pathology; Adolescent; Chromosome Aberrations; Chromosome Breakage; DNA Helicases/genetics; Diagnosis, Differential; Fatal Outcome; Growth Disorders/pathology; Humans; Karyotyping; Male; Mutation; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Progeria Type of study: Diagnostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2003 Type: Article Affiliation country: Netherlands

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