Parenthood among individuals with Turner syndrome: results of an online survey of attitudes towards pregnancy, adoption, and surrogacy Erin FalseyAllison L. CirinoAngela E. Lin Original Article 08 April 2022 Pages: 263 - 270
Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who? L. AlibertiI. GagliardiM. R. Ambrosio Original Article Open access 05 March 2022 Pages: 271 - 280
Attitudes and interest in incorporating BRCA1/2 cancer susceptibility testing into reproductive carrier screening for Ashkenazi Jewish men and women Melanie W. HardyBeth N. PeshkinMarc D. Schwartz Original Article 29 April 2022 Pages: 281 - 292
Families with complex needs: an inside perspective from young people, their carers, and healthcare providers Mădălina RaduRamona MoldovanAdriana Băban Original Article Open access 18 March 2022 Pages: 293 - 302
Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period Zandré BruwerSalwa Al UbaidaniKhalid Al-Thihli Original Article 18 February 2022 Pages: 303 - 311
Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom Alessia CostaVěra FrankováAlison Metcalfe Original Article Open access 06 May 2022 Pages: 313 - 327
Peripheral health workers’ knowledge and experience related to sickle cell disease: an in-depth interview study in six tribal-dominated districts of India Bontha V. BabuParikipandla SrideviYogita Sharma Original Article 01 February 2022 Pages: 329 - 338
Psychiatric symptoms in a Spanish sample with hereditary cancer risk Gema Costa-RequenaMercedes Garcia-GarijoÁngel Segura-Huerta Original Article 08 February 2022 Pages: 339 - 346
Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program Jirat ChenbhanichIvy RianoThomas Treadwell Original Article 01 March 2022 Pages: 347 - 354
QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa Laura CottinoVenesa SahibdeenAmanda Krause Original Article 15 March 2022 Pages: 355 - 363
Correction to: Co‑designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom Alessia CostaVěra FrankováAlison Metcalfe Correction Open access 01 July 2022 Pages: 365 - 369
