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

51 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia.
Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, de Matos RR, Binato R, Jordy FC, Abdelhay E, Ribeiro RC, Silva ML. Ney-Garcia DR, et al. Among authors: de souza mt, de matos rr. Leuk Lymphoma. 2012 Feb;53(2):342-4. doi: 10.3109/10428194.2011.613134. Epub 2011 Sep 29. Leuk Lymphoma. 2012. PMID: 21848362 No abstract available.
Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11.
Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, Capela de Matos RR, Pimenta G, Pulcheri W, Ribeiro RC, Abdelhay E, Silva ML. Ney-Garcia DR, et al. Among authors: de souza mt. Int J Hematol. 2012 Jan;95(1):112-4. doi: 10.1007/s12185-011-0981-x. Epub 2012 Jan 5. Int J Hematol. 2012. PMID: 22215484 No abstract available.
A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1 : The Contribution of Molecular Approaches for Revealing t(8;21) Variants.
de Matos RR, De Figueiredo AF, Liehr T, Alhourani E, De Souza MT, Binato R, Ribeiro RC, Silva ML. de Matos RR, et al. Among authors: de souza mt, de figueiredo af. Acta Haematol. 2015;134(4):243-5. doi: 10.1159/000431073. Acta Haematol. 2015. PMID: 26138995 No abstract available.
A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
de Figueiredo AF, Vieira TP, Liehr T, Bhatt S, de Souza MT, Binato R, Marques-Salles Tde J, Carboni E, Ribeiro RC, Silva ML, Abdelhay E. de Figueiredo AF, et al. Among authors: de souza mt. Leuk Res. 2012 Apr;36(4):e74-7. doi: 10.1016/j.leukres.2011.12.009. Epub 2012 Jan 18. Leuk Res. 2012. PMID: 22261229 No abstract available.
A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.
Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva ML. Ney-Garcia DR, et al. Among authors: de souza mt, de figueiredo af. Blood Cells Mol Dis. 2013 Feb;50(2):131-3. doi: 10.1016/j.bcmd.2012.09.005. Epub 2012 Oct 6. Blood Cells Mol Dis. 2013. PMID: 23044159 No abstract available.
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.
Capela de Matos RR, Othman M, Ferreira GM, Monteso K, de Souza MT, Rouxinol M, Melo JB, Carreira IM, Abdelhay E, Liehr T, Ribeiro RC, Silva M. Capela de Matos RR, et al. Among authors: de souza mt. Cancer Genet. 2022 Apr;262-263:16-22. doi: 10.1016/j.cancergen.2021.12.003. Epub 2021 Dec 22. Cancer Genet. 2022. PMID: 34974289
51 results