Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,109 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
KMT2A-MLLT1 and the Novel SEC16A-KMT2A in a Cryptic 3-Way Translocation t(9;11;19) Present in an Infant With Acute Lymphoblastic Leukemia.
de Matos RRC, Ferreira GM, Meyer C, Marschalek R, Larghero P, Ribeiro RC, Liehr T, Othman M, Bizarro MTSM, Sobral da Costa E, Land MGP, Abdelhay E, Binato R, Silva MLM. de Matos RRC, et al. Among authors: othman m. J Pediatr Hematol Oncol. 2022 Apr 1;44(3):e719-e722. doi: 10.1097/MPH.0000000000002386. J Pediatr Hematol Oncol. 2022. PMID: 34966090
GAS6 Oncogene and Reverse MLLT3-KMT2A Duplications in an Infant with Acute Myeloid Leukemia and a Novel Complex Hyperdiploid Karyotype: Detailed High-Resolution Molecular Cytogenetic Studies.
Capela de Matos RR, Ney Garcia DR, Cifoni E, Othman MAK, Tavares de Souza M, Carboni EK, Ferreira GM, Liehr T, Ribeiro RC, M Silva ML. Capela de Matos RR, et al. Among authors: othman mak, m silva ml. Cytogenet Genome Res. 2017;152(1):33-37. doi: 10.1159/000477108. Epub 2017 Jun 9. Cytogenet Genome Res. 2017. PMID: 28595195
An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia.
Monteso KCDA, Othman MAK, Capela de Matos RR, Ney Garcia DR, da Rocha MM, de Souza MT, Albagli LF, Liehr T, Land MGP, Silva MLM, Costa ES. Monteso KCDA, et al. Among authors: othman mak. J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e371-e374. doi: 10.1097/MPH.0000000000001776. J Pediatr Hematol Oncol. 2021. PMID: 32134839
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.
Capela de Matos RR, Othman MAK, Ferreira GM, Costa ES, Melo JB, Carreira IM, de Souza MT, Lopes BA, Emerenciano M, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Capela de Matos RR, et al. Among authors: othman mak. Cancer Genet. 2018 Feb;221:25-30. doi: 10.1016/j.cancergen.2017.12.002. Epub 2017 Dec 19. Cancer Genet. 2018. PMID: 29405993 Free article.
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
Capela de Matos RR, Ney Garcia DR, Othman MAK, Moura Ferreira G, Melo JB, Carreira IM, Meyer C, Marschalek R, Costa ES, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Capela de Matos RR, et al. Among authors: othman mak. Cytogenet Genome Res. 2019;157(4):213-219. doi: 10.1159/000499640. Epub 2019 Apr 12. Cytogenet Genome Res. 2019. PMID: 30974445
Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8.
De Souza MT, Vera-Lozada G, Othman M, Marques-Salles TJ, Pinto LW, da Rocha MM, Rouxinol S, Liehr T, Ribeiro RC, Hassan R, Silva MLM. De Souza MT, et al. Among authors: othman m. Ann Lab Med. 2018 Jan;38(1):63-66. doi: 10.3343/alm.2018.38.1.63. Ann Lab Med. 2018. PMID: 29071822 Free PMC article. No abstract available.
1,109 results