Gene editing and disabled people: a response to Felicity Boardman Iñigo de Miguel Beriain Short Communication 27 March 2020 Pages: 241 - 243
Letter to the editor. Gene editing and disabled people: a response to Iñigo de Miguel Beriain Felicity Boardman Letter to Editor Open access 30 April 2020 Pages: 245 - 247
Letter to the Editor: Time to update the language of genetics from the nineteenth to the twenty-first century: a response to Schmidtke and Cornel Neil SmallDan MasonJohn Wright Letter to Editor 03 May 2020 Pages: 249 - 251
Empowering newborn screening programs in African countries through establishment of an international collaborative effort Bradford L. Therrell JrMichele A. Lloyd-PuryearOn behalf of the faculty and speakers at the First Pan African Workshop on Newborn Screening, Rabat, Morocco, June 12-14, 2019 Original Article 15 May 2020 Pages: 253 - 268
The implementation of pharmacogenomics into UK general practice: a qualitative study exploring barriers, challenges and opportunities I. RafiI. CrinsonF. M. Walter Original Article Open access 28 May 2020 Pages: 269 - 277
A large family with CYLD cutaneous syndrome: medical genetics at the community level Anderson Pontes ArrudaAugusto César Cardoso-dos-SantosLavinia Schuler-Faccini Original Article 03 December 2019 Pages: 279 - 284
African American mothers’ attitudes towards genetic testing in the InterGEN study Michelle L. WrightKevin NewhallJacquelyn Y. Taylor Original Article 07 December 2019 Pages: 285 - 290
Online BRCA1/2 screening in the Australian Jewish community: a qualitative study Jeanette YuenNicole CousensLesley Andrews Original Article 26 December 2019 Pages: 291 - 302
Birth prevalence of congenital anomalies in the City of Buenos Aires, Argentina, according to socioeconomic level Ruben BronbergBoris GroismanRosa Liascovich Original Article 03 January 2020 Pages: 303 - 311
Prenatal detection of congenital anomalies and related factors in Argentina Maria Paz BidondoBoris GroismanPablo Barbero Original Article 03 January 2020 Pages: 313 - 320
Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor children Yelena P. WuLisa G. AspinwallSancy A. Leachman Original Article 18 January 2020 Pages: 321 - 329
Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care Siang Ing LeeNadeem QureshiStephen Weng Original Article Open access 22 January 2020 Pages: 331 - 338
Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment Amy A. LemkeJennifer ThompsonHenry M. Dunnenberger Original Article 04 February 2020 Pages: 339 - 350
Quality of life and comprehensive health supervision for children with Down syndrome in Thailand Kitiwan RojnueangnitPenrawee KhaosamleePak Sriplienchan Original Article 22 February 2020 Pages: 351 - 358
Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan Mónica AlvaradoGeorge E. TillerReina Haque Original Article 24 February 2020 Pages: 359 - 366
Applying Rogers’ framework to evaluate public awareness and knowledge of medical genetics in a developing country Hamid AsadollahiMahmoud VakiliReza Asadollahi Original Article 28 February 2020 Pages: 367 - 375
How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners W. R. H. EvansJ. TranterN. Qureshi Original Article Open access 03 March 2020 Pages: 377 - 386