Search Results - "genetic testing"

Diagnosis and Screening of Patients with Hereditary Transthyretin Amyloidosis (hATTR): Current Strategies and Guidelines by Benson MD, Dasgupta NR, Rao R

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Mammographies The Cultural Discourses of Breast Cancer Narratives by DeShazer, Mary K.

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Influence of Intra-ductal Carcinoma on Clinical Outcomes in Men with Prostate Cancer: Systematic Review and Meta-analysis by Jatinder Kumar, Muhammad Umar Alam, Karthik Tanneru, Shiva Gautam, Daniel Norez, Charu Shastri, Joseph Costa, Mark Bandyk, Hariharan Palayapalayam Ganapathi, Shahriar Koochekpour, Sanjeev Shukla, KC Balaji

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Risks in the Making Travels in Life Insurance and Genetics by Van Hoyweghen, Ine

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Ocular Motor and Vestibular Function in Neurometabolic, Neurogenetic, and Neurodegenerative Disorders by Aasef G. Shaikh

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Investigação citogenética e molecular de casos de autismo atendidos em um ambulatório universitário no sul do Brasil by Jaime Lin, Fernanda Coan Antune, Lalucha Mazzucchett, Maiara de Aguiar da Cost, Cinara Ludvig Gonçalves

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Assessing pharmacogenomic literacy in China through validation of the Chinese version of the Minnesota Assessment of Pharmacogenomic Literacy by Lusi Zhang, Shuqin Zhou, Josiah D. Allen, Fan Wang, Amy L. Pittenger, Jeffrey R. Bishop

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Additional germline findings from a tumor profiling program by Neda Stjepanovic, Tracy L. Stockley, Philippe L. Bedard, Jeanna M. McCuaig, Melyssa Aronson, Spring Holter, Kara Semotiuk, Natasha B. Leighl, Raymond Jang, Monika K. Krzyzanowska, Amit M. Oza, Abha Gupta, Christine Elser, Lailah Ahmed, Lisa Wang, Suzanne Kamel-Reid, Lillian L. Siu, Raymond H. Kim

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A national survey of first line antibiotic use in neonatal units - and the potential scope for iatrogenic sensorineural hearing loss prevention by J. Peterson, J. Peterson, L. Muddiman, F. Groves, N. Booth, W. G. Newman, W. G. Newman, J. H. McDermott, J. H. McDermott, A. Mahaveer

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Consequences of Fetal Cardiac Anomalies: A Two-Year Experience in a Tertiary Perinatology Center by Gokhan Bolluk, Isil Turan Bakirci, Mehmet Cok, Handan Turhan Karakus, Nur Benli Cok

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Diagnosis of GATA2 haplo-insufficiency in a young woman prompted by pancytopenia with deficiencies of B-cell and dendritic cell development by Allen Sanyi, David L. Jaye, Cecilia B. Rosand, Amanda Box, Chandrakasan Shanmuganathan, Edmund K. Waller

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Is hyperammonemia helpful in detecting syndromic tubulopathies with early extrarenal manifestations? A case report of Lowe's syndrome by Agnieszka Jędzura, Monika Dębowska, Piotr Adamczyk

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Cost-Effectiveness of Poly ADP-Ribose Polymerase Inhibitors in Cancer Treatment: A Systematic Review by Vivien Kin Yi Chan, Runqing Yang, Ian Chi Kei Wong, Ian Chi Kei Wong, Ian Chi Kei Wong, Xue Li, Xue Li, Xue Li, Xue Li

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Cleavage-stage human embryo arrest, is it embryo genetic composition or others? by Raoul Orvieto, Anat Jonish-Grossman, Sharon Avhar Maydan, Meirav Noach-Hirsh, Olga Dratviman-Storobinsky, Adva Aizer

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Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose? by Xiaoyi Cong, Tong Zhang, Zhenming Li, Xiaojin Luo, Liang Hu, Weiqiang Liu

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Intestinal obstruction due to a congenital mesenteric hernia in a newborn with cystic fibrosis: A case report by Maho Kurashima, Chadi Nahal, Christian Saliba, Raymond Okeke, Shin Miyata

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A Case Report of Pregnancy Complicated with Primary Hemophagocytic Lymphohistiocytosis by Chen Y, Huang X, Chen H, Tong J, Huang L, Su J, Deng L

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Phenotypic and Genetic Features that Differ Between Hereditary and Sporadic Melanoma: Results of a Preliminary Study from a Single Center from Turkey by Aysel Çakır, Gonca Elcin, Saadettin Kilickap, Özay Gököz, Zihni Ekim Taskiran, İsmail Celik

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Troublesome teeth, search for stones - Enamel-renal syndrome by Soumya Reddy, Niranjana Arumugam, Aparna Iyengar

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ADDITIVE EFFECT OF GENES POLYMORPHISM OF FOLATE CYCLE PROTEINS AND HOMOCYSTEIN LEVEL IN PATIENTS WITH PROLIFERATIVE DISEASES OF THE BREAST AS A POTENTIAL FACTOR OF THE RISK OF THRO... by Aleksandr V. Markovsky

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