Health systems across the country are making it easier for primary care clinicians to order genetic tests for patients who ...

“This innovative approach enables the identification of several genetic disorders, including sickle ... specialist at Al Qassimi Women’s and Children’s Hospital, told Khaleej Times at ...

A mother-of-four who lost two children to the same rare genetic condition says the fear of losing another child is "paralysing" as she calls for more research into sudden childhood death.

The new Kids First datasets advance our understanding of how genetics contribute to childhood cancers and congenital disorders, opening new doors for prevention and treatment.

A genetic study of childhood obesity in about 6,400 school-going children aged 9-18 years has ... role in obesity and related metabolic disorders,” she says. “Since genetic factors alone ...

Last year, at the Open Day of the CSIR-Centre for Cellular and Molecular Biology (CCMB), a biology research institute in Hyderabad, we administered a questionnaire to 78 students of Classes VIII-XII.

Marcelo was diagnosed with Treacher Collins syndrome, a rare condition affecting facial bone structure and cartilage. The genetic disorder left Marcelo without ears and with a smaller-than-normal ...

Clinical Director Rare Disease North East and Yorkshire Genomic Medical Services and Sheffield Children’s Consultant in Clinical Genetics, said:“Early identification of rare genetic disorders ...

A heartbroken couple have revealed how they aborted their healthy baby after mistakenly being told by NHS doctors that their newborn would have a serious genetic condition. Carly Wesson said she ...

The new Kids First datasets advance our understanding of how genetics contribute ... genomic sequencing data from children with pediatric cancer and congenital disorders. This data is freely ...