“A Call To Action”: The need for genetic counseling in Uganda by Tessa Adžemović, Kisakye Diana Kabbale, Eric Katagirya, John Mukisa, Misaki Wayengera

Subjects: “…Genetic counseling in Oman…”
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Genetic counseling development and milestone in Oman by Khalsa Al-Kharusi, Chantel Van Wyk, Mariya Al Hinai, Amel Al-Fori, Zandre Bruwer

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Genetic counseling in the Middle East: provider perspectives of patient attitudes and cultural challenges by Shruti Shenbagam, Alan Taylor, Ruchi Jain, Khalid Fakhro, Fowzan Alkuraya, Ahmad Abou Tayoun

Subjects: “…Genetic counseling…”
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Cancer genetic counseling in Chile: Addressing barriers, confronting challenges, and seizing opportunities in an underserved Latin American Community by Ricardo Fernández-Ramires, Sebastián Morales-Pison, Guilherme Gischkow Rucatti, César Echeverría, Esteban San Martín, Francisco Cammarata-Scalisi, Alexis Salas-Burgos, Daniela Adorno-Farias, Wilfredo Alejandro González-Arriagada, Yolanda Espinosa-Parrilla, Daniela Zapata-Contreras, Gabriela Norese, Conxi Lázaro, Sara González, Miguel Angel Pujana, Yasser Sullcahuaman, Sonia Margarit

Subjects: “…Genetic counseling…”
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A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program by Holly Canton, Rebecca Macintosh, Joanna Sweeting, Helen Mountain, Jodie Ingles, Amy Nisselle, Erin Turbitt, Alison McEwen, Laura Yeates

Subjects: “…Genetic counseling…”
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“Doing genetic literacy”: a discourse-oriented approach to literacy in genetic contexts by Zhengpeng Luo, Olga Zayts-Spence

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Molecular epidemiology and hematological thresholds for αβ-thalassemia: a retrospective cohort study in the Huizhou region of southern China by Dina Chen, Zhiyang Guan, Shaohui Huang, Zeyan Zhong, Hailin He, Guoxing Zhong, Zhiyong Wu, Jianhong Chen

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Telegenomics: Relevance in India by Krishnan Ganapathy

Subjects: “…genetic counseling and telemedicine…”
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The Role of Pedigree Charting and Analysis in Ophthalmology by Ria Ratna, Shailja Tibrewal

Subjects: “…genetic counseling…”
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Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand by Anaita Kanga-Parabia, Lucas Mitchell, Renee Smyth, Trisha Kapoor, Jaitika Duggal, Amy Pearn, Rachel Williams, Eliza Courtney, Emma Edwards, Michelle Bowman, Mithila Belekar, Clara Gaff, Amy Nisselle, Amy Nisselle, Amy Pearn, Anaita Kanga-Parabia, Ben Lundie, Claire Wong, N.S.W. Health, Clara Gaff, Australian Genomics, Helen Mountain, Jaitika Duggal, Jason Pinner, Lauren Hunt, Lyndon Gallacher, Rachel Williams, Sebastian Lunke, Yemima Burman, Alex Blackwell, Ana Rakonjac, Anaita Kanga-Parabia, Eliza Courtney, Emma Edwards, Emma Harrison, Janette Hayward, Lucas Mitchell, Lyndon Gallacher, Michelle Bowman, Michelle Cao, Mithila Belekar, Rachel Williams, Renee Smyth, Saraya Hogan, Trisha Kapoor

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BREAST AND/OR OVARIAN CANCER AS PART OF FAMILY CANCER SYNDROME by L. N. Lyubchenko, N. I. Pospelova, A. A. Parokonnaya, A. A. Luzhnikova, E. M. Chevkina

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Prenatal diagnosis of clinodactyly and its association with genetic syndromes: A case report by Themistoklis Loukopoulos, Athanasios Zikopoulos, Nikolaos Vlassis, Emmanouil Manolakos, Sotirios Sotiriou, Anastasia Vatopoulou, Fani Gkrozou, Anastasios Potiris, Sofoklis Stavros, Charikleia Skentou

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Autosomal dominant macrocephaly, acquired with impaired intellectual development: a report of an ultra-rare disease by Dinnar Yahya, Milena Stoyanova, Mari Hachmeriyan, Mariya Levkova

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Health-Promoting Lifestyle of Breast Cancer Patients and Family Members in a Chinese Genetic Counseling Clinic: A Cross-Sectional Study by Shengqun Hou, Liqin Chen, Xiaofang Lu, Cuixia Fu, Qianqian Yu, Tingting Su, Jiajia Qiu, Yun Li, Zhenqi Lu

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Assessment of Knowledge and Attitude of Breast and Ovarian Cancer Patients Regarding Hereditary Breast-Ovarian Cancer Syndrome at a Tertiary Cancer Institute: A Cross-Sectional Obs... by Raja Pramanik, Shubhra Vats, Sanchita Mitra, SVS Deo, Lalit Kumar, Ajay Gogia, Sachin Khurana, Atul Batra

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Analysis of Nursing Education Curricula in Spain: Integration of Genetic and Genomic Concepts by Estel·la Ramírez-Baraldes, Katerin Ariza-Martin, Daniel García-Gutiérrez, Cristina García-Salido

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A Novel Newborn Screening Program for Sickle Cell Disease in Nigeria by Aisha A. Galadanci, Umma A. Ibrahim, Yvonne Carroll, Yusuf D. Jobbi, Zubaida L. Farouk, Aisha Mukaddas, Nafiu Hussaini, Bilya Sani Musa, Lauren J. Klein, Michael R. DeBaun

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Acceptability of the ePOWER intervention: Managing previvors' cancer-related uncertainty and supporting decision making by Marleah Dean, Bethany Jowers, Claire Conley, Erica Camacho, Whitney Espinel, Kimberly A. Kaphingst

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Cardiologists' Perceptions of Cardiogenetic Testing and Management by W.H. Wilson Tang, MD, Quan M. Bui, MD, Allison L. Cirino, MS, CGC, Lisa Dellefave-Castillo, MS, CGC, Brendan J. Floyd, MD, PhD, MEd, Alejandra Guerchicoff, PhD, Marianna Guerchicoff, MD, Amit V. Khera, MD, MSc, Joshua W. Knowles, MD, PhD, Kristen Lafayette, MPP, Andrew P. Landstrom, MD, PhD, Daria W. Ma, MS, LCGC, MSHS, Ana Morales, MS, CGC, Kate M. Orland, MS, CGC, Daniel E. Pineda-Alvarez, MD, Siddharth K. Prakash, MD, PhD, Paul Theriot, BSBA, Melissa Dempsey, MS, CGC

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The dilemma of X-linked agammaglobulinemia carriers by Federica Pulvirenti, MD, PhD, Cinzia Milito, MD, PhD, Francesco Cinetto, MD, PhD, Giulia Garzi, MD, Germano Sardella, MD, Giuseppe Spadaro, MD, Francesca Lippi, MD, Valentina Guarnieri, MD, Bianca Laura Cinicola, MD, Maria Carrabba, MD, PhD, Daniele Guadagnolo, MD, Giovanna Fabio, MD, Baldassarre Martire, MD, Caterina Cancrini, MD, PhD, Giulia Lanzoni, MD, Andrea Finocchi, MD, PhD, Gigliola Di Matteo, MD, PhD, Eva Pompilii, MD, Simona Ferrari, BD, PhD, Isabella Quinti, MD, PhD

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