Genetic counseling in sickle cell disease: Insights from the Indian tribal population Pooja AggarwalDeepa Bhat Review 04 August 2023 Pages: 345 - 353
The beta thalassaemia trait in Jamaica G. R. SerjeantB. E. SerjeantA. E. Kulozik Research 30 June 2023 Pages: 355 - 360
Adolescents’ experiences and views of the national school-based thalassaemia screening programme in Malaysia: a qualitative study Huey Yee TanNorita HusseinTun Firzara Abdul Malik Research 01 July 2023 Pages: 361 - 369
“What if” should precede “whether” and “how” in the social conversation around human germline gene editing Diewertje HoutmanWendy GeuverinkSam Riedijk Research Open access 16 June 2023 Pages: 371 - 375
The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation Aaliyah HeywardKelsi HagertyNandini Govil Research 08 May 2023 Pages: 377 - 385
Nigerian parents’ perspectives on genetic testing in their children with genetic eye diseases Henrietta Ifechukwude MonyeOlusola Oluyinka OlawoyeTunji Sunday Oluleye Research 27 July 2023 Pages: 387 - 394
A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington’s disease Sarah VelissarisMarie-Claire DavisJulie C. Stout Research 17 July 2023 Pages: 395 - 405
Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive study Thamires Rosa dos SantosNicoly Stefani Sevalho CarlucciDébora Gusmão Melo Research 18 August 2023 Pages: 407 - 418
Life story of Iranian parents of a child with phenylketonuria: a qualitative study Marjan Mardani-HamoolehHaydeh Heidari Research 06 June 2023 Pages: 419 - 427
“Fruits of our past karma”: a qualitative study on knowledge and attitudes about congenital anomalies among women in Pune district, India Anita KarDipali DhamdhereAishwarya Medhekar Research 03 June 2023 Pages: 429 - 438
