The meiotic chromosome counts are reported in 10 species of the genus Cousinia including: C. adenostegia, C. antonowii, C. chaetocephala, C. dasylepis, C. eriobasis, C. freynii, C. prasina, C. rechingerorum, C. termei and C. trachyphyllaria from Iran. Specimens have been collected from different parts of Iran out of which, eight species are considered to be new and two provide confirmation of t...

the interpretation of supernumerary chromosome is important for genetic counseling and prognosis. here, we used snp array and conventional karyotyping method to identify a denovo marker chromosome originated from chromosome 22 and 11 in a newborn transferred to the neonatal intensive care unit of shahid sadoughi hospital in 2015.  clinical abnormalities identified in the newborn were dysmorphic...

in the present paper, the cytogenetic study including meiotic chromosome number and behavior along with pollen viability were performed in 4 populations of trigonella spruneriana boiss. this is the first cytogenetic report of the taxon. all populations are diploid and possess 2n = 2x = 16 chromosome number, which is consistent with the proposed basic number of x = 8. in addition, some meiotic i...

habit and pollen morphology were studied in four taxa belonging to astragalus sect. macrophyllium in iran. data obtained from pollen morphology support the phenetic grouping based on habit morphology. in addition, meiotic chromosome number and behavior were analyzed in two species of the section. the species were cytogenetically analyzed and found to be tetraploid and possess a 2n = 4x = 32 chr...

background: microdeletions of the azoospermia factor locus of the long arm of y chromosome are an etiological factor of severe oligozoospermia or azoospermia. objective: the aim of this study was to investigate the prevalence of y-chromosome microdeletions in azf region and their role in infertility in pakistani population. materials and methods: the type of deletions in azf locus were detected...

Ring chromosomes are rare chromosomal disorders that usually appear to occur de novo. A ring chromosome forms when due to deletion both ends of chromosome fuse with each other. Depending on the amount of chromosomal deletion, the clinical manifestations may be different. So, ring 18 syndrome is characterized by severe mental growth retardation as well as microcephaly, brain and ocular malformat...

This study concerns diploid chromosome numbers and karyotype analysis of nine species belonging to four sections (Vicilla, Cracca, Variegata and Anatropostylia) of the subgenus Vicilla of the genus Vicia (Fabaceae). The chromosome numbers of Vicia alpestris subsp. hypoleuca, V. aucheri, V. ciceroideae, V. gariensis, V. iranica, V. koeieana, V. rechingeri, V. sojakii and V. venulosa are reported...