Work

Maternal uniparental disomy of human chromosome 7

Year: 2001

Type: dissertation

Abstract: imprinting disorders Growth and development Cancer Methods for identifying imprinting in humans Parent-of-origin-specific DNA methylation Parent-of-origin-specific expression Location-based approach UNIPARENTAL DISOMY OF CHROMOSOME 7 MatUPD7 PatUPD7 Candidate chromosome 7 genes for SRS and growth retardation Imprinted genes PEG1/MEST COPG2, γ2-COP MEG1/GRB10 Genes not imprinted Human chromosome 7 and mouse homology

Source: Työväentutkimus Vuosikirja

Author: Katariina Hannula-Jouppi

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Suomen Lääketieteen Säätiö, Suomen Kulttuurirahasto, Päivikki ja Sakari Sohlbergin Säätiö, Lastentautien Tutkimussäätiö

OpenAlex ID: W2107428956

Cites: 274

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Related to: 10