Genoscoper Ltd. has published in cooperation with the researchers of University of Helsinki and Pennsylvania (USA) the most comprehensive study on canine hereditary disorders so far. The research ...

In this webinar, we will show you how to maximize your diagnostic yield of hereditary disorders with QCI Interpret. A clinical decision support platform powered by augmented molecular intelligence, ...

Genoscoper Ltd. has published in cooperation with the researchers of University of Helsinki and Pennsylvania (USA) so far the most comprehensive study on canine hereditary disorders. The research ...

The impairments associated with hereditary disorders of connective tissue (HDCTs), which may develop and progress over time, manifest throughout the body and affect functioning in every body system.

Hereditary spherocytosis (HS) is an inherited condition that affects the red blood cells. The cells are damaged as they pass through the spleen and do not survive as long as normal blood cells ...

More than 1,800 genes are known to cause hereditary disorders in humans. This review discusses the use of genetic medicines to treat monogenic hereditary disorders, and the technical, regulatory ...

Hereditary disorders of renal phosphate wasting are rare genetic diseases. Affected patients can be symptomatic during childhood or adulthood, depending on the disease entity. In this Review ...

Classic hereditary hemochromatosis is an autosomal recessive iron-overload disorder associated with mutation of the HFE gene, which is located on chromosome 6; in most cases the mutation is a ...

These disorders of the eating habits present themselves generally in adolescents who usually self restrict themselves, who are perfectionists, and have been outstanding for their intellectual ...

Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders. PLOS ONE, 2016; 11 (8): e0161005 DOI: 10.1371 ...