Search Results - "Laudicina, Alejandro"

Chromosomal location of 18S and 5S rDNA sites in Triportheus fish species (Characiformes, Characidae) by Diniz, Débora, Laudicina, Alejandro, Bertollo, Luiz Antonio Carlos

“…The location of 18S and 5S rDNA sites was determined in eight species and populations of the fish genus Triportheus by using fluorescent in situ hybridization…”
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Uses and limitations of two molecular cytogenetic techniques for the study of arrested embryos obtained through assisted reproduction technology by Muhlmann, Maria C, Laudicina, Alejandro O, Perandones, Claudia, Bertolino, Maria V, Marazzi, Andrea, Quintans, Carlos J, Donaldson, Monica, Bozzo, Walter, Pasqualini, Sergio

“…We studied chromosomal abnormalities in arrested embryos produced by assisted reproductive technology with fluorescence in situ hybridization (FISH) and…”
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An unusual translocation, t(1;11)(q21;q23), in a case of chronic myeloid leukemia with a cryptic Philadelphia chromosome by Gutiérrez, Leandro Germán, Noriega, María Fernanda, Laudicina, Alejandro, Quatrin, Mariana, Bengió, Raquel María, Larripa, Irene

“…Chronic myeloid leukemia (CML) is characterized by the translocation t(9;22)(q34;q11) [Philadelphia (Ph) chromosome). Although not frequently occurring,…”
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Chromosomal features of nucleolar dominance in hybrids between the Neotropical fish Leporinus macrocephalus and Leporinus elongatus (Characiformes, Anostomidae) by Hashimoto, Diogo Teruo, Laudicina, Alejandro, Bortolozzi, Jehud, Foresti, Fausto, Porto-Foresti, Fábio

“…In the present study, the chromosomal mechanisms of nucleolar dominance were analyzed in the hybrid lineage “Piaupara,” which resulted from crossing the…”
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Origin and molecular organization of supernumerary chromosomes of Prochilodus lineatus (Characiformes, Prochilodontidae) obtained by DNA probes by Voltolin, Tatiana Aparecida, Laudicina, Alejandro, Senhorini, José Augusto, Bortolozzi, Jehud, Oliveira, Cláudio, Foresti, Fausto, Porto-Foresti, Fábio

“…In Prochilodus lineatus B-chromosomes are visualized as reduced size extra elements identified as microchromosomes and are variable in morphology and number…”
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Phenotypic variability in 47, XXX patients: Clinical report of four new cases by Goldschmidt, Ernesto, Márquez, Marisa, Solari, Andrea, Ziembar, María I, Laudicina, Alejandro

“…The 47, XXX karyotype has a frequency of 1 in 1000 female newborns. However, this karyotype is not usually suspected at birth or childhood. These patients are…”
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Variabilidad fenotípica en pacientes 47, XXX: Presentación de cuatro casos nuevos by Goldschmidt, Ernesto, Márquez, Marisa, Solari, Andrea, Ziembar, María I., Laudicina, Alejandro

“…El síndrome 47, XXX se debe a un cromosoma extra del par sexual; su incidencia es de 1 en 1000 recién nacidas vivas. Sin embargo, este síndrome no suele…”
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