Detection of <i>M. tuberculosis</i> Using Cartridge-Based Technology in Patients with Negative Sputum Microscopy Results in a Regional Laboratory by P. I. Eliseev, E. I. Nikishova, A. Yu. Krupskaya, V. I. Shtraukh, E. S. Khimova, A. O. Maryandyshev

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COLQ-Mutant Congenital Myasthenic Syndromes by J Gordon Millichap

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MODY in Siberia – molecular genetics and clinical characteristics by Alla Konstantinovna Ovsyannikova, Oksana Dmitrievna Rymar, Elena Vladimirovna Shakhtshneider, Elena Nikolaevna Voropaeva, Dinara Evgenevna Ivanoshchuk, Mikhail Ivinovich Voevoda

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X-Linked Charcot-Marie-Tooth Disease in 93 Patients by J Gordon Millichap

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Pontocerebellar Hypoplasia Type 1 by J Gordon Millichap

Subjects: “…molecular genetic testing…”
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Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update by Deepti Narasimhaiah, Megha S Uppin, Prajnya Ranganath

Subjects: “…molecular genetic testing…”
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Molecular testing panel in colorectal cancer by Yi Ding, Guoli Chen

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KRAS-mutated non-small cell lung cancer: new therapy strategies by K. K. Laktionov, K. A. Sarantseva, L. A. Nelyubina, S. V. Gamayunov, E. A. Kolesnikova, M. G. Gordiev

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Incidence of familial hypercholesterolemia in patients with early manifestations of coronary artery disease: data from a Russian multicenter study and meta-analysis by A. A. Rogozhina, A. O. Averkova, E. A. Zubova, L. O. Minushkina, V. A. Brazhnik, O. N. Ivanova, M. A. Chichkova, N. R. Khasanov, E. D. Kosmacheva, O. I. Boeva, D. A. Zateyshchikov

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A Rare Cause of Neonatal Hypotonia: First Case of Autosomal Recessive Fast-Channel Congenital Myasthenic Syndrome Type 1B in Albania by Eda Jazexhiu-Postoli, Sonila Tomori, Gladiola Hoxha, Mirela Tabaku, Aferdita Tako, Ada Simeoni, Sonila Biba, Paskal Cullufi

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Phenotypic vs. genetic cascade screening for familial hypercholesterolemia: A case report by Anastasia V. Blokhina, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Marina V. Klimushina, Anastasia A. Zharikova, Anastasia A. Zharikova, Evgeniia A. Sotnikova, Vasily E. Ramensky, Vasily E. Ramensky, Oxana M. Drapkina

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Multimorbidity in Pediatric Dermatology: Clinical Case by Nikolay N. Murashkin, Alexander I. Materikin, Eduard T. Ambarchian, Roman V. Epishev, Leonid A. Opryatin, Roman A. Ivanov, Daria S. Kukoleva, Daria G. Kuptsova, Alexander A. Pushkov, Marina Yu. Pomazanova, Yana V. Kozyr

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Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report by Tsuyoshi Murata, Toma Fukuda, Aya Kanno, Hyo Kyozuka, Akiko Yamaguchi, Hiromi Shimizu, Takafumi Watanabe, Keiya Fujimori

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The role of influenza viruses in the development of severe acute respiratory infection in patients admitted to Yekaterinburg hospitals during 2017–2018 epidemic season by Aleksandr V. Alimov, Svetlana S. Smirnova, Evgenia V. Lelenkova, Aleksandr Yu. Markaryan, Ivan V. Vyalykh, Vladislav K. Verevshchikov, Andrey B. Komissarov, Anna A. Sominina

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Molecular-genetic testing of single-nucleotide polymorphism C-33T of IL4 gene in children with recurrent episodes of acute obstructive bronchitis. by O. V. Kens, O. Z. Gnateyko, N. S. Lukyanenko, V. I. Bergtravm

Subjects: “…molecular genetic testing…”
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Classification and Interpretation for 11 FBN1 Variants Responsible for Marfan Syndrome and Pre-implantation Genetic Testing (PGT) for Two Families Successfully Blocked Transmission... by Songchang Chen, Songchang Chen, Songchang Chen, Songchang Chen, Hongjun Fei, Hongjun Fei, Junyun Zhang, Junyun Zhang, Yiyao Chen, Yiyao Chen, Hefeng Huang, Hefeng Huang, Hefeng Huang, Daru Lu, Chenming Xu, Chenming Xu, Chenming Xu

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A case of Niemann – Pick disease type C by Sergei Anatolyevich Klyushnikov, O R Smirnov, E Yu Zakharova

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CHARCOT-MARIE-TOOTH DISEASE by Lea Leonardis, Janez Zidar, Borut Peterlin

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Modern algorithms of geno-phenotypic diagnosis of tuberculosis in Ukraine by O.A. Zhurylo, A.I. Barbova

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THE SURGICAL STAGE OF PULMONARY TUBERCULOSIS TREATMENT USING MOLECULAR-GENETIC METHODS TO TEST SUSCEPTIBILITY TO RIFAMPICIN by A. V. Golovnin, A. L. Khanin, V. I. Golovnin

Subjects: “…molecular genetic tests for mtb…”
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