Results 11 to 20 of about 7,482 (176)

Híbridos de passifloras UESC-HD13 confirmados pela análise de RAPD, morfologia e citogenética

open access: yesOrnamental Horticulture, 2007
Esse trabalho teve como objetivos descrever híbridos UESC-HD13 e confirmar sua natureza híbrida utilizando marcador molecular RAPD, análise da segregação de caraterísticas morfológicas e da variação ...
Magarete Magalhães Souza   +11 more
doaj   +1 more source

Outcome of fetuses with increased risk of chromosomal anomalies, based on nuchal translucency measurement [PDF]

open access: yes, 2005
PURPOSE: to evaluate the outcome of fetuses with risk of chromosomal anomalies over 1:300, based on the nuchal translucency measurement, according to the Fetal Medicine Program.
Camano, Luiz   +4 more
core   +4 more sources

Prevalência de duplicação interna in tandem/fms-receptor tirosino-quinase (DIT/FLT3) em pacientes com leucemia mielóide aguda de novo classificados conforme grupos citogenéticos de risco [PDF]

open access: yes, 2009
CONTEXT AND OBJECTIVE: The mechanism involved in leukemogenesis remains unclear and more information about the disruption of the cell proliferation, cell differentiation and apoptosis of neoplastic cells is required.
Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]   +2 more
core   +1 more source

Gonadal dysgenesis and tumors: genetic and clinical features [PDF]

open access: yes, 2005
Gonadal dysgenesis comprises a clinical spectrum of anomalies in patients with female, ambiguous or male phenotype, absent or impaired puberty and karyotype with or without Y chromosome and/or chromosome markers.
Bianco, Bianca Alves Vieira   +2 more
core   +3 more sources

Polimorfismo cromossômico em Capsicum chinense Jacq. Chromosome polymorphism in Capsicum chinense Jacq.

open access: yesCiência Rural, 2011
Este estudo teve como objetivo determinar o cariótipo de quatro acessos de Capsicum chinense procedentes do Rio Janeiro, Bahia, Pará e Maranhão. Em todos os acessos, foram observados 2n=2x=24 cromossomos. Polimorfismo cromossômico foi observado no acesso
Sérgio Alessandro Machado Souza   +2 more
doaj   +1 more source

Karyotype and NOR-banding of mitotic chromosomes of some Vitis L. species

open access: yesRevista Brasileira de Fruticultura, 2011
Chromosome studies were performed in V. champinii, V. cinerea, V. girdiana, V. labrusca, V. rotundifolia, V. rupestris and V. vinifera with the purpose of species characterization using chromosome morphometric data and NOR banding.
Neiva Izabel Pierozzi
doaj   +1 more source

Morphometric analysis on chromosomes of tropical Pinus species.

open access: yesCiência Florestal, 2009
Foram realizados estudos citogenéticos em Pinus oocarpa Schiede ex Schltdl., Pinus patula Schltdl. & Cham. e nas procedências Jócon Yoro, Las Camelias e San Rafael del Norte do Pinus tecunumanii Eguiluz & J. P.
Lília Rosário Ribeiro   +4 more
doaj   +1 more source

High incidence of chromosomal numerical abnormalities by multicentromeric FISH in multiple myeloma patients [PDF]

open access: yes, 2007
This study aimed to characterize genetic alterations by interphase multicentromeric FISH focusing on chromosomal numerical abnormalities and using some locus specific probes for the most frequent aberrations found in the disease, in a homogeneous cohort ...
Almeida, Manuella S. S.   +7 more
core   +3 more sources

Clinical and speech, hearing and language pathology manifestations on Turner Syndrome: bibliographical study [PDF]

open access: yes, 2011
TEMA: síndrome genética e achados fonoaudiológicos. OBJETIVO: descrever as manifestações clínicas e fonoaudiológicas em indivíduos com a Síndrome de Turner CONCLUSÃO: foram levantados 23 artigos sobre a Síndrome de Turner dos quais 7 discorriam sobre a ...
Abramides, Dagma Venturini Marques   +1 more
core   +1 more source

Two-hit model of leukemogenesis in the evolution of polycythemia vera to acute myeloid leukemia [PDF]

open access: yes, 2009
Polycythemia vera (PV) is a chronic myeloproliferative disorder that can evolve to marrow fibrosis or acute leukemia (AML). Cytogenetic alterations can be detected in around 25% of patients at diagnosis and in up to 50% of those with progression.
Chauffaille, Maria de Lourdes Lopes Ferrari   +2 more
core   +1 more source

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