MOLECULAR STRUCTURE OF AMYOTROPHIC LATERAL SCLEROSIS IN RUSSIAN POPULATION by N. Yu. Abramycheva, E. V. Lysogorskaya, Yu. S. Shpilyukova, A. S. Vetchinova, M. N. Zakharova, S. N. Illarioshkin

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Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients by Elena Bonora, Claudio Graziano, Fiorella Minopoli, Elena Bacchelli, Pamela Magini, Chiara Diquigiovanni, Silvia Lomartire, Francesca Bianco, Manuela Vargiolu, Piero Parchi, Elena Marasco, Vilma Mantovani, Luca Rampoldi, Matteo Trudu, Antonia Parmeggiani, Agatino Battaglia, Luigi Mazzone, Giada Tortora, IMGSAC, Elena Maestrini, Marco Seri, Giovanni Romeo

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Genomic surveillance of SARS-CoV-2 variants using pooled WGS by Inho Park, Yoonjung Kim, Min Hyuk Choi, Kyung-A Lee

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DETECTION OF MUTATIONS RELATED TO HEREDITARY CANCER IN RELATIVES OF BREAST CANCER PATIENTS by G. A. Paul, N. A. Matyash, E. E. Pisareva, M. S. Anisimenko, A. E. Kozyakov, S. P. Kovalenko

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Detection and analysis of MSX1 gene mutations in two families with non-syndromic tooth agenesis by DING Tingting, LIU Haochen

Subjects: “…tooth agenesis|gene mutation|muscle segment homeobox 1|genetic disorder|developmental anomaly|mutation screening|exome sequencing|genetic counseling…”
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Feasible and Rapid Screening of <i>IDH1/2</i> and <i>FLT3-TKD2</i> Mutations by High-Resolution Melting for Patients with Acute Myeloid Leukemia by José Vicente Gil, Sandra de las Heras, Alberto Miralles, Claudia Sargas, Marta Llop, Rebeca Rodríguez-Veiga, Laura Torres-Miñana, Blanca Boluda, Isabel Cano-Ferri, Evelyn Acuña-Cruz, Irene Navarro, Pilar Lloret-Madrid, Pau Montesinos, Eva Barragán

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