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A translocation t(5;15)(q15;q11-13) infant case with acute lymphoblastic leukemia and literature review: Prognosis implications
(2012)
Infant acute lymphoblastic leukemia (ALL) represents poor prognosis despite intensive chemotherapy. Rearrangements of chromosome 11q23 are not observed in 34% of the cases. Infant ALL patients with t(5;15)(p15;q11-13) are ...
Past, present and future of cytogenetics in Costa RicaPasado, presente y futuro de la citogenética en Costa Rica
(Universidad de Costa Rica, 2004)
Sensorineural deafness in two infants: A novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes
(2004)
Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. cardinal signs in trisomies 22 subtypes: Distal trisomy 22 has been described in more than 15 individuals. The features are ...
Protective in vivo effect of curcumin on copper genotoxicity evaluated by comet and micronucleus assays
(2007)
Curcumin is a phytochemical with antiinflammatory, antioxidant and anticarcinogenic activities. Apparently, curcumin is not genotoxic in vivo, but in vitro copper and curcumin interactions induce genetic damage. The aim ...
Revisitando o desvendamento da etiologia da síndrome de turnerRevisiting establishment of the etiology of turner syndrome
(Casa de Oswaldo Cruz, Fundação Oswaldo Cruz, 2015)
Chromosome instability in a patient with recurrent abortions
(2009)
Chromosomal aberrations are one of the recognized possible etiologic genetic causes of recurrent spontaneous abortions. Increased chromosome instability without constitutional chromosome abnormalities is uncommon in these ...
Chromosome instability in a patient with recurrent abortions
(2009)
Chromosomal aberrations are one of the recognized possible etiologic genetic causes of recurrent spontaneous abortions. Increased chromosome instability without constitutional chromosome abnormalities is uncommon in these ...
Ataxia telangiectasia. Diagnosis and monitoring in a series of four cases [Ataxia telangiectasia. Diagnóstico y seguimiento en una serie de cuatro casos]
(2013)
Ataxia telangiectasia (AT) is a chromosomal instability syndrome with autosomal recessive inheritance, it is caused by more than 500 mutations of the ATM gene, which is involved in the cellular response to DNA damage. The ...