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JCEM Case Reports|January 17, 2025
Diagnosing Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome and a Novel <i>GATA3</i> VariantAnisley Valenciaga, Pamela Brock, Benjamin O'Donnell, et al.
Familial Cancer|January 7, 2021
Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromesJennifer L Anderson, Robert Pilarski, Lawrence Kirschner, et al.
Familial Cancer|October 14, 2017
Penetrance of a rare familial mutation predisposing to papillary thyroid cancerDonika Saporito, Pamela Brock, Heather Hampel, et al.
Familial Cancer|February 14, 2020
Co-occurrence of multiple endocrine neoplasia type 4 and spinal neurofibromatosis: a case reportPamela Brock, Jean Bustamante Alvarez, Amir Mortazavi, et al.
Journal of Genetic Counseling|August 14, 2019
Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test resultsBrooke M Nightingale, Shelly R Hovick, Pamela Brock, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2016
Genome-Wide Expression Screening Discloses Long Noncoding RNAs Involved in Thyroid CarcinogenesisSandya Liyanarachchi, Wei Li, Pearlly Yan, et al.
American Journal of Human Genetics|April 30, 2024
Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtypeEmily A DeBoy, Anna M Nicosia, Sandya Liyanarachchi, et al.
Thyroid : Official Journal of the American Thyroid Association|December 8, 2023
Presumed Pathogenic Germ Line and Somatic Variants in African American Thyroid CancerZachary A Hurst, Sandya Liyanarachchi, Pamela Brock, et al.
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