Search Results - "genetic counseling"

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  1. 81
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    Personalized and Precision Medicine 2022

    Published 2023
    Subjects: “…genetic counselling…”
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  2. 82
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    OnkoRiskNET: a multicenter, interdisciplinary, telemedicine-based model to improve care for patients with a genetic tumor risk syndrome by Johanna Tecklenburg, Beate Vajen, Susanne Morlot, Petra Anders, Paula Memenga, Elena Link, Eva Baumann, Sarah Wölffling, Evelin Schröck, Anke Katharina Bergmann, Brigitte Schlegelberger

    Published 2022
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  3. 83
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    A REPORT OF 4 CASES OF CHROMOSOME ABNORMALITIES IN 115 FAMILIES WITH CONSANGUINEOUS MARRIAGE by H.Khavari- Khorasani

    Published 1992
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  4. 84
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    Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants by Adelyn Beil, Whitney Hornsby, Wendy R. Uhlmann, Rajani Aatre, Patricia Arscott, Brooke Wolford, Kim A. Eagle, Bo Yang, Jennifer McNamara, Cristen Willer, J. Scott Roberts

    Published 2021
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  5. 85
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    Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosis by Laynie Dratch, Weiyi Mu, Elisabeth McCarty Wood, Brianna Morgan, Lauren Massimo, Cynthia Clyburn, Tanya Bardakjian, Murray Grossman, David J. Irwin, Katheryn A.Q. Cousins

    Published 2023
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  6. 86
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    A New Model for Providing Cell-Free DNA and Risk Assessment for Chromosome Abnormalities in a Public Hospital Setting by Robert Wallerstein, Andrea Jelks, Matthew J. Garabedian

    Published 2014
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  7. 87
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    Self-efficacy and self-management strategies in acute intermittent porphyria by Marte H. Hammersland, Aasne K. Aarsand, Sverre Sandberg, Janice Andersen

    Published 2019
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  8. 88
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    Congenital Hypothyroidism 3-Year Follow-Up Project: Region 4 Midwest Genetics Collaborative Results by Kupper A. Wintergerst, Erica Eugster, Karen Andruszewski, Mary Kleyn, Nancy Vanderburg, Joe Sockalosky, Ram Menon, Sharon Linard, Suzanne Kingery, Susan R. Rose, Julie Moore, Gina Gembel, Lisa Gorman

    Published 2018
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  9. 89
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    Study Of The Genetic Disorders Of Couples Attending Genetics Clinic, Imam Khomeini Hospital Complex During 1995 To 2004 by Mostafa Rabieyan, Reza Safdari, Cyrus Azimi

    Published 2011
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  10. 90
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    Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus... by Wen-Xu Yang, Hong Pan, Song-Tao Wang, Lin Li, Hai-Rong Wu, Yu Qi

    Published 2016
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  11. 91
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    Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autis... by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

    Published 2021
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  12. 92
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    Study of the Genetic Disorders of Couples Attending Genetics Clinic, Imam Khomeini Hospital Complex During 1995 to 2004 by Reza Safdari, Mostafa Rabieyan, Cyrus Azimi

    Published 2012
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  13. 93
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    Prenatal diagnosis of hereditary diffuse gastric cancer: a case report by Jun Xiao, Hui Li, Fenggui Xue, Zhifei Luo, Yanyang Pang

    Published 2023
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  14. 94
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    Metastasis of Pregnancy-Associated Breast Cancer (Suspected to Be Hereditary Breast and Ovarian Cancer) to the Brain, Diagnosed at 18 Weeks' Gestation: A Case Report and Review of... by Tomohiro Okuda, Sakura Yamamoto, Seiki Matsuo, Hisashi Kataoka, Jo Kitawaki

    Published 2016
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  15. 95
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    Germline genetic testing reveals pathogenic variants in uterine serous carcinoma patients by Katelyn Tondo-Steele, Kara J. Milliron, Jean H. Siedel, Shitanshu Uppal, Sofia D. Merajver, Karen McLean

    Published 2024
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  16. 96
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    Complexities of Clinical Genetics Consultation: An Interprofessional Clinical Skills Workshop by Jodi D. Hoffman, Rachel Thompson, Kathleen B. Swenson, Shoumita Dasgupta

    Published 2020
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  17. 97
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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

    Published 2014
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  18. 98
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    Prenatal Diagnosis of Complex Copy Number Variants in the Fetus and Associated Cytogenetic Findings in Parents by Wei Wang, Jing Wang, Ye Shi, Bin Zhang

    Published 2023
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  19. 99
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    Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiency by Yitong Lu, Shaozhi Zhao, Xiaohui He, Hua Yang, Xiaolei Wang, Chen Miao, Hongwei Liu, Xinwen Zhang

    Published 2022
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  20. 100
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    Order from chaos: a case report of a healthy live birth from a genetically "chaotic" embryo by Joanna Lin, M.D, Wendy Vitek, M.D, Erin L. Scott, M.D., Ph.D

    Published 2022
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