Adverse Events in Genetic Testing: The Fourth Case Series.

Autor: Farmer MB; From the My Gene Counsel, LLC, Branford, CT.; Department of Genetics University of Alabama at Birmingham, Birmingham, AL., Bonadies DC; From the My Gene Counsel, LLC, Branford, CT., Mahon SM; Saint Louis University, St Louis, MO., Baker MJ; Penn State Health, Hershey, PA., Ghate SM; St Vincent Hospital Medical Genetics Clinic, Green Bay, WI., Munro C; Children's Hospital of Pittsburgh, Pittsburgh, PA., Nagaraj CB; Cincinnati Children's Hospital Medical Center, Cincinnati, OH., Besser AG; NYU Fertility Center, NYU Langone Health, New York, NY., Bui K; Prisma Health, Greenville, SC., Csuy CM; Novant Health Presbyterian Medical Center, Charlotte, NC., Kirkpatrick B; Watershed DNA, Crozet, VA., McCarty AJ; Children's Hospital of Pittsburgh, Pittsburgh, PA.; PerkinElmer Genomics, Pittsburgh, PA., McQuaid SW; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL., Sebastian J; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA., Sternen DL; Department of Laboratories and Patient-Centered Laboratory Utilization Guidance Services, Seattle Children's Hospital, Seattle, WA., Walsh LK; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA., Matloff ET; From the My Gene Counsel, LLC, Branford, CT.

Publikováno v: Cancer journal (Sudbury, Mass.) [Cancer J] 2019 Jul/Aug; Vol. 25 (4), pp. 231-236.

Postgraduate training in Cancer Genetics—a cross-specialty survey exploring experience of clinicians in Ireland.

Autor: K McHugh, Jana, Offiah, Gozie, Daly, Sean, El Beltagi, Nazmy, Barry, Michael Kevin, O'Reilly, Seamus, P McVeigh, Terri

Publikováno v: Irish Journal of Medical Science; Jun2022, Vol. 191 Issue 3, p1427-1434, 8p

Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes.

Autor: Butz, Henriett, Blair, Jo, Patócs, Attila

Publikováno v: Endocrine (1355008X); Mar2021, Vol. 71 Issue 3, p641-652, 12p

Genetic testing for hereditary gastrointestinal cancer syndromes: Interpreting results in today's practice.

Autor: Powers, Jacquelyn M., Ebrahimzadeh, Jessica E., Katona, Bryson W.

Publikováno v: Current Treatment Options in Gastroenterology; Dec2019, Vol. 17 Issue 4, p636-649, 14p

Rare Genetic Disorders : Advancements in Diagnosis and Treatment

Autor: Muhammad Umair, Misbahuddin Rafeeq, Qamre Alam

This book introduces different Rare Genetic Disorders (RGDs), and challenges in their diagnosis. The chapters of the book discuss the emerging research and clinical approaches for the diagnosis of rare genetic disorders. It further reviews the future