rye (secale cereale) chromosome 1rs harbors multiple genes including lr26, sr31, yr9 and pm8 conferring disease resistance and tolerance to abiotic stresses. the introgression of the rye 1r chromosome short arm has enormously contributed to increase of genetic diversity in wheat. utilization of such translocations in breeding programs demands identification of wheat germplasm possessing the whe...

cytogenetic studies were performed on 150 cases of down's syndrome (ds) in iran. the standard trisomy 21 was found in 132 (88 % ) and translocation-trisomy 21 (+21) in 18 (12%) patients, i.e., t(21,21) in 1(0.63%) and mosaicism in 17(11.33%) cases. the comparison of the frequencies for mosaicism between different populations such as denmark, hungary, egypt, iraq, india, australia and iran ...

rapid expansion of the industrial sector adds more effluent into the agricultural land and in the vicinity of industry, which possesses the major threat of land contamination and environmental degradation. the present study was conducted to determine toxic metal concentration in fly ash and metal accumulation potential of the saccharum munja and cynodon dactylon, the two main grass species grow...

one of the major causes of spontaneous abortion before the fourth month of pregnancy is chromosomal abnormalities. we report an unusual case of a familial balanced chromosomal translocation in a consanguineous couple who experienced 4 spontaneous abortions. chromosomal studies were performed on the basis of g-banding technique at high resolution and revealed 46, xx, t (16 6) (p12 q26) and 46, x...

the short arm of rye (secale cereale l.) chromosome 1 (1rs), besides being part of the rye genome, is present in many hundred wheat cultivars as either 1rs.1bl or 1rs.1dl wheat-rye translocation. in this study, the distribution of the wheat–rye translocation was examined in 33 iranian winter and spring wheat cultivars, nine of which had a known donor of 1rs.1bl translocation and the other 24 we...

chromosomal defects are relatively frequent in infertile men however, translocations between the y chromosome and autosomes are rare and less than 40 cases of y-autosome translocation have been reported. in particular, only three individuals has been described with a y;21 translocation, up to now. we report on an additional case of an infertile man in whom a y;21 translocation was associated wi...

background: the human aml1 gene, located on chromosome 21, can be fused to the aml1- eight-twenty-one (eto) oncoprotein on chromosome eight, resulting in a t(8;21)(q22;q22) translocation. acute myeloid leukemia (aml) associated with this translocation is considered a distinct aml with a favorable prognosis. due to the various incidences of the translocation, which is associated with geographic ...

A case mongolism due to "hereditary trans­location ·· is presented and discussed. The mother of the patient showed a Karyogram with 45-XX and G/D translocation. She had no stigmata. She had an abortio when she was 19 years old.  In the second pregnancy the amniotic fluid was gained by amniocentesis. The Karyogram showed G/D translocation mongolism. The Karyo­gram of the child's father was norm...

this case report presents a coincidence of trisomy 18 and balanced robertsonian translocation (13;14). aneuploidy was suspected based on anomalies detected in ultrasound scan and confirmed with karyotype. in a 31 years-old healthy woman with a history of one miscarriage, second trimester ultrasound scan reported iugr (<3rd percentile) with normal amniotic fluid, bilateral choroid plexus cysts, ...

jak2 is a tyrosine kinase that plays an important role in the signaling pathways of many hematopoietic growth factor receptors. a single acquired point mutation – v617f – in jak2 occurs in the great majority of patients with polycythemia vera (pv) and approximately half of the patients with idiopathic myelofibrosis (imf) or essential thrombocythemia (et). in contrast, the jak2-v617f mutation is...