"This is my boy's health! Talk straight to me!" perspectives on accessible and culturally safe care among Aboriginal and Torres Strait Islander patients of clinical genetics services

by Dalach, Philippa, Savarirayan, Ravi, Baynam, Gareth, McGaughran, Julie, Kowal, Emma, Massey, Libby, Jenkins, Misty, Paradies, Yin, Kelaher, Margaret
Published in International journal for equity in health

Clinical genetics provider real-time workflow study

by McPherson, Elizabeth, Zaleski, Christina, Benishek, Katrina, McCarty, Catherine A., Giampietro, Philip F., Reynolds, Kara, Rasmussen, Kristen
Published in Genetics in medicine

Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population

by Martínez-Barrios, Estefanía, Cesar, Sergi, Cruzalegui, José, Hernandez, Clara, Arbelo, Elena, Fiol, Victoria, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar, Sarquella-Brugada, Georgia
Published in Biomedicines

Clinical genetics of Kallmann syndrome

by Dodé, C, Hardelin, J.-P
Published in Annales d'endocrinologie

The composition and capacity of the clinical genetics workforcein high-income countries: a scoping review

by Dragojlovic Nick, Kennedy, Borle, Kopac Nicola, Ellis, Ursula, Birch, Patricia, Shelin, Adam, Friedman, Jan M, Nisselle Amy, Elliott, Alison M, Lynd, Larry D
Published in Genetics in medicine

Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands

by Vrijenhoek, T., Tonisson, N., Kääriäinen, H., Leitsalu, L., Rigter, T.
Published in Journal of community genetics

Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening

by Hansen, Christina A., Reiter, Aaron W., Wildin, Robert S.
Published in Journal of community genetics

Inherited Isolated Dystonia: Clinical Genetics and Gene Function

by Dauer, William
Published in Neurotherapeutics

Clinical Genetics today

by Tizzano Ferrari, Eduardo
Published in Medicina clínica (English ed.)

eP441: Evaluation of growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening

by Hansen, Christina, Reiter, Aaron, Wildin, Robert
Published in Genetics in medicine

eP480: Project ECHO for pediatric genetics in Mississippi: Expanding access to the clinical genetics workup for autism and intellectual disability

by Boothe, Emily, Waldrop, John Michael, Kirmse, Brian
Published in Genetics in medicine

Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2022"

Published in Hereditary cancer in clinical practice

Clinical genetics involved in monogenic forms of hypertension in Chinese patients with early-onset hypertension and hypokalemia

by Fan, P, Zhang, D, Yang, K.Q, Zhang, Y, Lu, Y.T, Luo, F, Tian, T, Liu, Y.X, Zhou, X.L
Published in European heart journal

Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study

by Veatch, Olivia J, Steinle, Jacob, Hossain, Waheeda A, Butler, Merlin G
Published in BMC medical genomics

Milestones for medical students completing a clinical genetics elective

by Press, Katharine R., Bodurtha, Joann
Published in Genetics in medicine

The cost of rejection: an internal audit of the clinical genetics service active triage pathway at CHI Crumlin, Ireland

by Coleman, John, Kavanagh, Karl, Lynch, Sally Ann, Bradley, Lisa
Published in Irish journal of medical science

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

by Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky J J, van den Hout, Mirjam C G N, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan D H, Kamps, Rick, Kockx, Christel E M, de Koning, Bart, Kriek, Marjolein, Deprez, Ronald Lekanne Dit, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Weiss, Janneke Marjan, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred F J, den Dunnen, Johan T, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin
Published in European journal of human genetics : EJHG

Clinical genetics and genomic medicine in Qatar

by Al‐Dewik, Nader, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Othman, Amna, AlMulla, Mariam, Sulaiman, Reem Al, Musa, Sara, Abdoh, Ghassan, El‐Akouri, Karen, Solomon, Benjamin D., Ben‐Omran, Tawfeg
Published in Molecular genetics & genomic medicine

ACMG Standards and Guidelines for fragile X testing: a revision to the disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics and Genomics

by Monaghan, Kristin G, Lyon, Elaine, Spector, Elaine B
Published in Genetics in medicine

Clinical genetics

Published in Archives of disease in childhood