Detalhe da pesquisa
1.
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study.
J Genet Couns
; 33(1): 4-14, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37051800
2.
Fatal melanoma with a novel MYO5A-BRAF fusion and small associated conventional nevus: A case report and review of literature.
J Cutan Pathol
; 49(9): 808-812, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35596628
3.
Positive and negative professionalism experiences of genetic counseling students in the United States and Canada.
J Genet Couns
; 30(2): 478-492, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33010196
4.
Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis.
Cytogenet Genome Res
; 160(11-12): 671-679, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33535208
5.
AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.
Hum Mol Genet
; 24(18): 5093-108, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26085575
6.
Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.
J Med Genet
; 53(10): 672-680, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27208205
7.
Signet-ring cell lymphoma: clinicopathologic, immunohistochemical, and fluorescence in situ hybridization studies of 7 cases.
Ann Diagn Pathol
; 26: 38-42, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28038709
8.
Prognostic relevance of integrated genetic profiling in acute myeloid leukemia.
N Engl J Med
; 366(12): 1079-89, 2012 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22417203
9.
Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine.
Birth Defects Res A Clin Mol Teratol
; 103(1): 45-50, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25131804
10.
Cyclophosphamide/fludarabine nonmyeloablative allotransplant for acute myeloid leukemia.
Am J Hematol
; 90(2): 97-9, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25345651
11.
ZMIZ1::ABL1 Fusion: An Uncommon Molecular Event With Clinical Implications in Pediatric Cancer.
Arch Pathol Lab Med
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38749501
12.
Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism.
Genet Med
; 15(9): 729-32, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23492874
13.
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.
Am J Med Genet A
; 161A(12): 2953-63, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24123848
14.
Fluorescence in situ hybridization (FISH) as an aid for the diagnosis of graft-versus-host disease in two multivisceral organ transplant patients.
Am J Dermatopathol
; 35(4): 496-502, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23694825
15.
Improvement of diagnosis in children with Burkitt lymphoma in Kenya: feasibility study for the implementation of fluorescence in situ hybridisation testing for MYC and the MYC/IGH translocation.
Ecancermedicalscience
; 17: 1505, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37113725
16.
Establishment and characterization of a novel cell line derived from human thymoma AB tumor.
Lab Invest
; 92(11): 1564-73, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22926645
17.
Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia.
Blood
; 116(16): 2915-20, 2010 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20606166
18.
Glioblastoma occurring at the site of a previous medulloblastoma following a 5-year remission period.
Neuropathology
; 32(5): 543-50, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22151431
19.
Malignant gastrointestinal neuroectodermal tumour arising in the extrahepatic bile ducts; a rare neoplasm in an unusual anatomic location.
BMJ Case Rep
; 15(7)2022 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35858740
20.
Laboratory and Clinical Implications of Incidental and Secondary Germline Findings During Tumor Testing.
Arch Pathol Lab Med
; 146(1): 70-77, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33769456