Detalhe da pesquisa
1.
OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.
J Med Genet
; 60(6): 620-626, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36368868
2.
A homozygous PAX3 mutation leading to severe presentation of Waardenburg syndrome with a prenatal diagnosis.
Prenat Diagn
; 35(13): 1379-81, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26443304
3.
Exon 7 deletion in the bcr-abl gene is frequent in chronic myeloid leukemia patients and is not correlated with resistance against imatinib.
Mol Cancer Ther
; 9(11): 3083-9, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21045136
4.
Monosomal karyotype routinely defines a poor prognosis subgroup in acute myeloid leukemia and is frequently associated with TP53 deletion.
Leuk Lymphoma
; 53(2): 336-7, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21823831