About PWS Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15.

Completed in 2003, the Human Genome Project gave us the first sequence of the human genome, albeit based on DNA from a small ...

Understand the impact of azoospermia on male fertility. Learn about the causes, diagnosis, and treatment options for men with ...

A chromosome analysis is performed for all three approaches to identify other chromosome abnormalities as recommended by the ACMG 7, 8 for all individuals with mental retardation or birth defects ...

IVF offers women over 40 advanced fertility treatments that help overcome age-related challenges, providing hope and ...

Psilocybin improved longevity and health markers in mice and cells. The findings reveal unexpected systemic benefits. As the ...

In Morocco’s educational system – already ranked among the lowest globally – thousands of children with Trisomy 21 exist in ...

The 1000 Genomes Project (2007–2015) collected DNA samples from diverse human populations across five continents to analyse genetic variation from humans across the globe. Using advanced sequencing ...

According to a report prepared by the genetic unit of the department of pediatrics in the All India Institute of Medical Sciences, all pregnant women should undergo a blood test between 15 and ... the ...

Van Andel Institute scientists have developed an improved technique to comprehensively profile DNA methylation in single cells, an advance that will help researchers better study the role of ...

The results devastated Mai and her husband: Gao had Hutchinson-Gilford Progeria Syndrome (HGPS), a rare genetic disorder caused by a mutation on chromosome 1. The condition causes accelerated aging in ...