Estudo do polimorfismo 609C>T no gene NQO1 em leucemias agudas pediátricas.

Título:

Estudo do polimorfismo 609C>T no gene NQO1 em leucemias agudas pediátricas.

Autor:

Márcia Rodrigues Amorim

Ano:

2006

Revista:

Revista Brasileira de Hematologia e Hemoterapia (Impresso)

ISSN:

15168484

Idioma:

Português

Buscar essa publicação no Google Acadêmico

Publicações com a mesma autoria

Feasibility of Using Molecular Genetic Tools in a Congenital Malformation Registry.

Down syndrome: the aggravation of COVID-19 may be partially justified by the expression of TMPRSS2

Is there a familial link between Down's syndrome and neural tube defects? Population and familial survey

DNA extraction from fixed cytogenetic cell suspensions

COVID-19 and SARS-CoV-2: Despite the vaccination, new targets/drugs for treatment and the virus cycle mechanisms still have to be continually investigated

Non-Latin European descent could be a requirement for association of NTDs andMTHFR variant 677C?>?T: A meta-analysis

No association of the polyhistidine tract polymorphism of the ZIC2 gene with neural tube defects in a South American (ECLAMC) population

AUTISMO NO BRASIL: UMA REVISÃO SOBRE ESTUDOS EM NEUROGENÉTICA

MTHFR 677C→T And 1298A→C POLYMORPHISMS IN CHILDREN WITH DOWN SYNDROME AND ACUTE MYELOID LEUKEMIA IN BRAZIL

Are we getting closer to the role of one carbon metabolism and methylation in the onset of Down syndrome?