Work

Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23

Year: 1999

Type: article

Source: Cytogenetic and Genome Research

DOI: 10.1159/000015322

Authors: Y. Franke, R.J. Peoples, U. Francke

Institutions: Stanford Medicine, Stanford University, Howard Hughes Medical Institute

Language: English

Topic: Williams Syndrome Research

Subfield: Developmental Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Human Genome Research Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G170485756, G4770299518, INTRACHROMOSOMAL GENE MAPPING, G802038413, MOLECULAR ANALYSIS OF THE WILLIAMS SYNDROME DELETION

OpenAlex ID: W2040584895

FWCI: 1.368

Cites: 52

Cited by: 59

Related to: 10