Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference34 articles.
1. Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13
2. Frequency of 13q Abnormalities Among 203 Patients With Retinoblastoma
3. Retinoblastoma in a Patient with a 13qxp Translocation
4. The Incidence of Retinoblastoma
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1. Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability;Ophthalmic Genetics;2022-06-06
2. Sex, gender, and retinoblastoma: analysis of 4351 patients from 153 countries;Eye;2021-07-16
3. A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report;BMC Medical Genomics;2019-12
4. Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46,X,t(X;22)(p11.2;q11.2);Journal of Medical Genetics;2003-09-01
5. Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.;Journal of Medical Genetics;1993-09-01
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