Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome. | Genomics;65(3): 234-42, 2000 May 01. | MEDLINE

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Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.

Squire, J A; Li, M; Perlikowski, S; Fei, Y L; Bayani, J; Zhang, Z M; Weksberg, R.

Affiliation

Squire JA; Ontario Cancer Institute, The Hospital for Sick Children, Toronto, Canada.

Genomics ; 65(3): 234-42, 2000 May 01.

Article in En | MEDLINE | ID: mdl-10857747

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Insulin-Like Growth Factor II / Genomic Imprinting / RNA, Untranslated / DNA Replication / Muscle Proteins Limits: Female / Humans / Male Language: En Journal: Genomics Journal subject: GENETICA Year: 2000 Document type: Article Affiliation country: Country of publication:

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Collection: 01-internacional Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Insulin-Like Growth Factor II / Genomic Imprinting / RNA, Untranslated / DNA Replication / Muscle Proteins Limits: Female / Humans / Male Language: En Journal: Genomics Journal subject: GENETICA Year: 2000 Document type: Article Affiliation country: Country of publication: