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Tetrasomy 8 in a patient with chronic lymphocytic leukemia
(ELSEVIER SCIENCE INC, 2010)
We report a case of a 47-year-old man diagnosed with chronic lymphocytic leukemia (CLL) with two extra copies of chromosome 8. Classical cytogenetic analysis by the immunostimulatory combination of DSP30 and interleukin 2 ...
Tetrasomy 3q26.32-q29 Due To A Supernumerary Marker Chromosome In A Child With Pigmentary Mosaicism Of Ito
(Soc Brasil GeneticaRibeirão Preto, 2016)
Tetrasomy 15Q11-Q13 identified by fluorescence in situ hybridization in a patient with autistic disorder
(2002-06-01)
We report a female child with tetrasomy of the 15q11-q13 chromosomal region, and autistic disorder associated with mental retardation, developmental problems and behavioral disorders. Combining classical and molecular ...
Tetrasomy 15Q11-Q13 identified by fluorescence in situ hybridization in a patient with autistic disorder
(2002-06-01)
We report a female child with tetrasomy of the 15q11-q13 chromosomal region, and autistic disorder associated with mental retardation, developmental problems and behavioral disorders. Combining classical and molecular ...
The variable phenotype in tetrasomy 18p syndrome. A propos of a subtle dysmorphic case
(2010)
Tetrasomy 18 is a rare chromosomal syndrome. Its frequency is 1/40,000 newborns and more than 40 cases have been reported. In this paper we report a 25-month-old female patient referred for chromosome examination essentially ...
Molecular and Cytogenetic Analyses on Brazilian Youths with Pervasive Developmental Disorders
(2002-02-01)
The Pervasive Developmental Disorders (PDDs) constitute a group of behavioral and neurobiological impairment conditions whose main features are delayed communicative and cognitive development. Genetic factors are reportedly ...