Interstitial deletion of the short arm of chromosome 4 in a boy with mild psychomotor retardation and dysmorphism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03586.x/fullpdf
Reference12 articles.
1. Localization of the human dihydropteridine reductase gene to band p15.3 of chromosome 4 by in situ hybridization;Brown;Genomics,1987
2. Proximal 4p-deletion: phenotype differs from classical 4p- syndrome;Francke;J. Pediatr.,1977
3. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome;Fryns;Ann. Génét.,1989
4. Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome;Gusella;Nature,1985
5. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion;Hirschhorn;Hum. Genet.,1965
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1. Familial 4p Interstitial Deletion Provides New Insights and Candidate Genes Underlying This Rare Condition;Genes;2023-03-03
2. A boy with 13.34-Mb interstitial deletion of chromosome 4p15;Medicine;2017-12
3. RBPJ is disrupted in a case of proximal 4p deletion syndrome with epilepsy;Brain and Development;2014-06
4. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14);Gene;2013-10
5. A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis;American Journal of Medical Genetics Part A;2011-09-09
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