Detalhe da pesquisa
1.
Clinical utility and cost-effectiveness analysis of chromosome testing concomitant with chromosomal microarray of patients with constitutional disorders in a U.S. academic medical center.
J Genet Couns
; 31(2): 364-374, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34397147
2.
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma.
Mol Vis
; 18: 705-13, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22509100
3.
Rare double-hit with two translocations involving IGH both, with BCL2 and BCL3, in a monoclonal B-cell lymphoma/leukemia.
Mol Cytogenet
; 8: 101, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26719766