25 Mb deletion of 13q13.3→q21.31 in a patient without retinoblastoma
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference5 articles.
1. Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma;Cowell;Hum. Genet.,1988
2. Molecular basis of low-penetrance retinoblastoma;Harbour;Arch. Ophthalmol.,2001
3. Mutation and cancer: statistical study of retinoblastoma;Knudson;Proc. Natl. Acad. Sci. USA,1971
4. Interstitial deletion 13q syndromes: a report on two unrelated patients;Serena-Lungarotti;Hum. Genet.,1979
5. Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis;Vermeesch;J. Histochem. Cytochem.,2005
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1. Chromosomal DNA balance in human stem cell line 4BL;Cytology and Genetics;2016-07
2. De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver;Italian Journal of Pediatrics;2014-01-16
3. Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion;Journal of Medical Genetics;2007-09-14
4. Genotype–phenotype correlations in hereditary familial retinoblastoma;Human Mutation;2007
5. From chromosomes to molecular karyotyping;European Journal of Medical Genetics;2005-07
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