Body weight (BW) and carcass traits are complex and important economic traits that may benefit from the implementation of MAS. The objective of the current study was to identify QTL associated with BW and carcass traits in an experimental half-sib cross of Japanese quails selected for BW at 4 weeks of age. Body weight and carcass traits were measured in the F2 population. Total F2 individuals a...

Background: Microdeletions of the long arm of the chromosome Y are the most common molecular genetic cause of severe infertility in men which affect three regions of AZFa, AZFb and AZFc (Azoospermia factor). These regions contain various genes involved in spermatogenesis. The effect of ethnicity on the patterns of Y chromosome microdeletions has not been extensively studied, particulary in Iran...

erodium (geranaiceae) species are distributed in different habitats of iran. some species are of medicinal importance while some are well known weeds. there are no chromosome counts for erdoium species of iran. chromosome numbers are given for six taxa of erodium (geraniaceae) from iran: e. cicutarium (2n=36), e. ciconium(2n=18), e. malacoides (2n=20), e. moschatum (2n=20), e. neuradifolium (2n...

background: chromosomal disorders are the most common cause of first trimester spontaneous abortion. among the human chromosomes, chromosome no.9 was the most common structural chromosomal variant and it is not thought to be of any functional importance, which often considers as a normal variation in structural polymorphisms, nevertheless there are some studies which claim that there is an asso...

The chromosomal spread and karyotype of Anjak (Schizocypris altidorsalis) from Hamoun Lake were determined using tissue squashing techniques with an injection of 1 mL/100 g body weight of 0.01% colchicines solution. Kidney and gill epithelia tissues were removed and used for karyotype analysis. The analysis of 145 chromosome spreads revealed the diploid chromosome number of this fish, 2n=48 and...

Oculo-auriculovertebral dysplasia (Goldenhar) is a congenital syndrome. Its phenotype differs from craniofacial anomalies to cardiac, vertebral or central nervous system defects. This syndrome is rare and its etiology is not apparent yet. Pericentric inversion of chromosome 9 is one of the most common structural balanced chromosomal aberrations with its incidences 15% to 25%. Herein we present ...