Interstitial microdeletion of the 1p34.3p34.2 region

Author:

Jacher Joseph E.1ORCID,Innis Jeffrey W.1

Affiliation:

1. Department of Pediatrics and Communicable Diseases; Division of Pediatric Genetics; Metabolism & Genomic Medicine; University of Michigan; Ann Arbor Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference15 articles.

1. Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities;Dagklis;Molecular Cytogenetics,2016

2. Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica;Delisi;American Journal of Medical Genetics,2002

3. SNIP1 is a candidate modifier of the transcriptional activity of cMyc on E box-dependent target genes;Fujii;Molecular Cell,2006

4. SNIP1 inhibits NF-kappa-B signaling by competing for its binding to the C/H1 domain of CBP/p300 transcriptional co-activators;Kim;Journal of Biological Chemistry,2001

5. A novel Smad nuclear interacting protein, SNIP1, suppresses p300-dependent TGF-beta signal transduction;Kim;Genes and Development,2000

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