A Mouse Single-Copy Gene,Gtf2i,the Homolog of HumanGTF2I,That Is Duplicated in the Williams–Beuren Syndrome Deletion Region
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference21 articles.
1. Basic local alignment search tool;Altschul;J. Mol. Biol.,1990
2. The PROSITE database, its status in 1995;Bairoch;Nucleic Acids Res.,1996
3. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome;Ewart;Nature Genet.,1993
4. LIM-kinase 1 hemizygosity implicated in impaired visuospatial constructive cognition;Frangiskakis;Cell,1996
5. Human GRB-IRbeta/GRB10: Splice variants of an insulin and growth factor receptor-binding protein with PH and SH2 domains;Frantz;J. Biol. Chem.,1997
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1. Mapping Genetically Controlled Neural Circuits of Social Behavior and Visuo-Motor Integration by a Preliminary Examination of Atypical Deletions with Williams Syndrome;PLoS ONE;2014-08-08
2. Expression of the transcription factor, TFII-I, during post-implantation mouse embryonic development;BMC Research Notes;2010-07-20
3. Copy number variants at Williams–Beuren syndrome 7q11.23 region;Human Genetics;2010-05-01
4. Characterization of a novel interaction between transcription factor TFII-I and the inducible tyrosine kinase in T cells;European Journal of Immunology;2009-08-21
5. The genomic basis of the Williams – Beuren syndrome;Cellular and Molecular Life Sciences;2008-11-26
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