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Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
Runte, M; Färber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Bürger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K.
Affiliation
  • Runte M; Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany.
Eur J Hum Genet ; 9(7): 519-26, 2001 Jul.
Article in En | MEDLINE | ID: mdl-11464243
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Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Chromosomes, Human, Pair 15 / Angelman Syndrome / DNA Methylation Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Germany
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Chromosomes, Human, Pair 15 / Angelman Syndrome / DNA Methylation Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Germany