A female infant with trisomy 9 in 58% of her cells is reported. Multiple congenital malformations were present, but she had normal psychomotor development. A pericentric inversion involving a portion of the centromeric heterochromatin of chromosome 9 was identified in the patient and her mother. This variant chromosome 9 was present in duplicate in the trisomic line. Since similar variants of 9...

Drimia is a heterogeneous, poorly understood genus that requires major rearrangement. Chromosome behavior of gigantea and viridula; two species in D. altissima complex was studied for karyotypes transmission extra chromosomes pair pollen viability. Meristematic cells at the root tips viridula were by conventional cytogenetic karyotype analysis. numbers 2n = 22 20 viridula, respectively. Extra c...

conclusions both the cases discussed in our study have inv(9) as the sole abnormality and are found to confer a relatively poor prognosis. case presentation we present the case of a chronic myeloid leukemia (cml) patient who showed intermittent relapse on treatment, with a rare appearance of clones with dual inversion (9) breakpoints [inv(9)(p22q34); inv(9)(p11q21)]. we also present the first r...

The chromosomal polymorphism defined by variations of some regions a person (the constitutive heterochromatin and the short arms acrocentric chromosomes (13 to 15 21 - 22)) sometimes highlighted problems with regard their safety pathogenicity. Polymorphisms are usually found in same family transmitted dominant Mendelian. Chromosome 9 inversion is frequent phenomenon that cytogeneticists conside...