review the literature on handedness, dichotic listening and anatomical asymmetry in schizophrenia and concluded that there was strong evidence for decreased cerebral lateralisation. As they point out, the implication is that finding the locus of the gene for cerebral dominance could unravel the genetic predisposition to schizophrenia. Procopio (2001) raises a number of points relevant to the fi...

Objective: Estimation of genetic parameters for Kleiber ratio (KR) and genetic trends for pre-weaning weights of Arabi sheep has not been previously conducted.Methods: Data and pedigree information were collected at the Khuzestan Ramin Agricultural and Natural Resources University, Animal Science Research Station, located in southwest Iran, from 2001 to 2008. (Co)variance components and corresp...

The objective of the current study was to estimate the genetic parameters for body weight traits at different ages in Iran-Black sheep. Data collected during a 24-year period (1984-2008) on body weight were used to model the growth trajectory and estimate genetic parameters. Studied traits were birth weight (BW), weaning weight at 3 months of age (WW), 6 months weight (6MW), 9 months weight (9M...

Declines in honeybee populations have been a recent concern. Although causes of the declines remain unclear, environmental factors may be responsible. We focused on the potential environmental determinants of local populations of wild honeybees, Apis cerana japonica, in Japan. This subspecies has little genetic variation in terms of its mitochondrial DNA sequences, and genetic variations at nuc...

introduction oculocutaneous albinism (oca) is a genetically heterogeneous autosomal recessive genetic disorder that is characterized by reduced or completely absent pigmentation in the hair, skin, and eyes. conclusions a novel homozygous mutation, the deletion of exons 1 - 5 on the tyr gene, was found on the molecular genetic testing of this patient. exon 1 - 5 deletion on tyr causes a lack of ...

It was with great interest that we read the recently published artic1e by de Rubens Figueroa et al1 in REVISTA ESPAÑOLA DE CARDIOLOGÍA. The article contained a report that the most frequently observed isolated cardiac defects in Mexican children with Down syndrome are atrial septal defects and ventricular septal defects. This observation, which has been described previously,2 contrasts with rep...

A combination of genetic variations, epimutations and environmental factors may be involved in the etiology of complex neurodevelopmental disorders like schizophrenia. To study such disorders, we use apomorphine-unsusceptible (APO-UNSUS) Wistar rats and their phenotypic counterpart apomorphine-susceptible (APO-SUS) rats that display a complex phenotype remarkably similar to that of schizophreni...