The present study reports the chromosome number and meiotic behaviour of 14 populationsbelonging to four taxa of Anchusa subgenus Buglossum Gusul. from Iran. All populationsshowed the chromosome number 2n= 4x= 32. It is the first meiotic study for A. subg.Buglossum. We discuss some habit form and evolutionary aspect in the light of cytogeneticdata. The origin of polyploidy (auto-allopolyploidy)...

in order to obtain maximum information from magnetic and gravity anomaly maps, application of an edgedetection method is necessary. in this regard two commonly used methods are derivative filters and local phase filters. in this paper, a matlab code is expanded to combine an analytic signal filter and a tilt angle filter as a new edge detection filter called asta filter. this method was demonst...

Testicular biopsies from eight men with abnormal karyotypes have been examined for histological and cytogenetic evidence of disturbances of meiosis. Quantitative analysis of this material showed one, with a 13;14 Robertsonian translocation, to have apparently normal spermatogenesis. Three patients, one with a 47,XYY and two with 45,XY, inv 9 karyotypes, had an overall depression of spermatogene...

This is the first case description of the association of Klippel-Feil Syndrome (KFS), Tourette Syndrome (TS), Motor Stereotypies, and Obsessive Compulsive Behavior, with chromosome 22q11.2 Duplication Syndrome (22q11DupS). Neuropsychiatric symptoms in persons with 22q11.2 deletion, including obsessive compulsiveness, anxiety, hyperactivity, and one prior case report of TS, have been attributed ...

In this study, 115 samples taken from the stream sediments were analyzed for concentrations of As, Co, Cr, Cu, Ni, Pb, W, Zn, Au, Ba, Fe, Mn, Sr, Ti, U, V and Zr. In order to outline mineralization-derived stream sediments, various mapping techniques including fuzzy factor score, geochemical halos and fractal model were used. Based on these models, concentrations of Co, Cr, Ni, Zn, Ba, Fe, Mn, ...

background: several studies have assessed the correlation of fetal choroid plexus cyst (cpc) and the risk of congenital anomalies, but few ones have discussed isolated cpc (with no other abnormal sonographic finding). objective: the aim of this study was to determine the outcome of isolated fetal choroid plexus cyst and to specify its clinical significance. materials and methods: this cross sec...

Variations in the human karyotype have been found in association with a variety of congenital anomalies and also in the normal population (Miller and Mukherjee, 1962; Court Brown, 1967). Court Brown's population studies (1967) have revealed that between 2 and 3%o of the normal adult population has a karyotype with structural autosomal variations. Occasionally, homologous autosomes reveal differ...