Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia-Reference-Cited by-同舟云学术

Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia

Published:2017-03 Issue:2 Volume:39 Page:e85-e91
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Borges Maria L.R.,Capela de Matos Roberto R.,Amaral Bethânia d.A. Silva,Soares-Ventura Eliane M.,Leite Edinalva P.,Silva Mariluze O. d.,Cornélio Maria T.M. Nogueira,Silva Maria L. M.,Liehr Thomas,Marques-Salles Terezinha d. J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

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2. Fanconi anaemia: review article;Tischkowitz;J Med Genet,2003

3. Chromosomal aberrations associated with clonal evolution and leukemic transformation in Fanconi anemia: clinical and biological implications;Meyer;Anemia,2012

4. Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor;Tönnies;Blood,2003

5. Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with Fanconi anemia: morphologic and cytogenetic characteristics;Cioc;Am J Clin Pathol,2010

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1. Clinical and cytogenetic profile of Fanconi anemia diagnosed after implementation of mitomycin C cytogenetic test in the state of Pernambuco, Brazil;Hematology, Transfusion and Cell Therapy;2023-01

2. An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia;Molecular Cytogenetics;2018-07-11