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Cytogenetic evaluation of 20 primary breast carcinomas
(1997-11-03)
Chromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. ...
Cytogenetic evaluation of 20 primary breast carcinomas
(1997-11-03)
Chromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. ...
Velocardiofacial syndrome with a rare t(2;22)
(2007-07-01)
Rearrangements involving chromosomes 2 and 22 were described not only as acquired abnormalities in a variety of human neoplasias but also in the constitutional karyotype suggesting the existence of a greater fragility in ...
The Cytogenetic Examination as a Tool for the Diagnosis of Chromosomal Disorders
(Sociedad Chilena de Anatomía, 2011)
Caracterización citogenético-molecular de enfermedades genéticas en el Hospital Base de Puerto Montt
(2011)
Background: Chromosome aberrations (CA) are the main etiology of multiple
congenital malformations, recurrent abortions and intellectual disability (ID) specifi
cally of moderate and severe degree. They account for 0.3 ...
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 ...
Caracterización citogenético-molecular de enfermedades genéticas en el Hospital Base de Puerto Montt
(Sociedad Médica de Santiago, 2011)