Acute lymphoblastic leukemia in a nine-year-old girl with isodicentric chromosome 15 syndrome

Author:

Antonucci Roberto,Vacca Nadia,Ghisu Elisa,Acquaviva Gloria,Cosmi Carlo,Marinaro Anna Maria,Locci Cristian,Fozza Claudio

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference9 articles.

1. The inv dup15 or idic15 syndrome: a clinically recognizable neurogenetic disorder;Battaglia;Brain Dev,2005

2. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints;Amos-Landgraf;Am J Hum Genet,1999

3. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients;Christian;Am J Hum Genet,1995

4. Parental imprinting and human disease;Lalande;Ann Rev Genet,1996

5. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication;Cook;Am J Hum Genet,1997

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1. B‐cell lymphoblastic leukemia in an adolescent with Dravet syndrome;Pediatric Blood & Cancer;2023-04-19

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