Search
Now showing items 21-30 of 448
DUPLICATION OF THE SHORT ARM OF THE X-CHROMOSOME IN MOTHER AND DAUGHTER
(Springer, 1993-05-01)
An 11-year-old girl with short stature, mental retardation, and mild dysmorphic features was found to have an inverted duplication of most of the short arm of the X chromosome [dic inv dup(X)(qter --> p22.3 = p22.3 --> ...
Meiotic behaviour and B chromosomes in Argentine populations of Chrysolaena verbascifolia (Vernonieae: Asteraceae)
(Taylor and Francis Ltd., 2017-01)
Four populations of Chrysolaena verbascifolia (Vernonieae: Asteraceae) from localities in Argentina were cytologically analysed for meiotic behaviour and pollen viability. This is the first meiotic analysis in the species. ...
Meiotic behaviour and B chromosomes in Argentine populations of chrysolaena verbascifolia (vernonieae: asteraceae)
(Taylor and Francis Ltd, 2017-01)
Four populations of Chrysolaena verbascifolia (Vernonieae: Asteraceae) from localities in Argentina were cytologically analysed for meiotic behaviour and pollen viability. This is the first meiotic analysis in the species. ...
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 ...
A new molecular screening tool for the detection of chromosomal abnormalities in donkeys
(Wiley Blackwell Publishing, Inc, 2019-03)
Chromosomal abnormalities are a major cause of infertility and reproductive problems in equids. Nowadays, their detection is rising due to the use of new diagnostic tools based on molecular markers instead of karyotyping. ...
Wide Clinical Variability in Cat Eye Syndrome Patients: Four Non-Related Patients and Three Patients from the Same Family
(KARGERBASEL, 2012)
A small supernumerary marker chromosome (sSMC) derived from chromosome 22 is a relatively common cytogenetic finding. This sSMC typically results in tetrasomy for a chromosomal region that spans the chromosome 22p arm and ...
Relevância da genética na etiologia do autismo
(2000-07-01)
Autism constitutes one of the most important pathologies of the pervasive developmental disorders (PDDs). It has early age-onset and is characterized by delay and deviance of social, communicative and cognitive development. ...