Detalhe da pesquisa
1.
Pediatric acute myeloid leukemia with t(7;21)(p22;q22).
Genes Chromosomes Cancer
; 58(8): 551-557, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30706625
2.
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay.
Cytogenet Genome Res
; 159(1): 19-25, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31487712
3.
Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1.
Am J Med Genet A
; 170(10): 2580-6, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27549381
4.
Validation of MYC and BCL6 rapid break apart digital fluorescence in situ hybridization assays for clinical use.
Int J Clin Exp Pathol
; 16(4): 76-85, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37168512
5.
Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.
Mol Syndromol
; 11(3): 125-129, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32903844
6.
Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors.
Eur J Med Genet
; 62(1): 9-14, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29698806
7.
Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.
J Clin Pathol
; 71(4): 372-378, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29197855