Pure trisomy 10p resulting from an extra ring chromosome: Characterization by methods of advanced molecular cytogenetics
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference8 articles.
1. Pure trisomy 10p involving an isochromosome 10p
2. Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH.
3. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: Cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection
4. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12)
5. Coverage of chromosome 6 by chromosome microdissection: generation of 14 subregion-specific probes
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1. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26
2. Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies;Journal of Tropical Pediatrics;2015-10-27
3. The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype;Systems Biology in Reproductive Medicine;2015-08-13
4. An unusual de novo duplication 10p/deletion 10q syndrome: The first case in Korea;Journal of Genetic Medicine;2015-06-30
5. Complete trisomy 10p resulting from an extra stable telocentric chromosome;American Journal of Medical Genetics Part A;2012-05-24
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