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Issue Date	Title	Author(s)
2020	A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome	Abdulsamad Wafa, Faten Moassass; Suher Almedani, Thomas Liehr; Kathleen Wilhelm
2020	Association of L432V (rs1056836) polymorphism of the CYP1B1 gene with the increased risk of colorectal cancer in the population of Central Russia	Moskalev, A. S.
2020	2q14 de novo interstitial deletion in a girl with intellectual disabilities and malformations	Alvarez, Y. B.; Garcia, A. G.; Rosales, L. M.; Méndez-Rosado, L. A.
2020	Aplastic anemia, clinical implications and DNA damage in workers with occupational exposure to aromatic hydrocarbons in Rio de Janeiro	Melo, K.; Santiago, F.; Lucena, S. B.; Silvestre, R. T.; Bravo, M.
2020	Increased usage of Smartphones in Medicine, an opportunity for Medical Cytogenetics	Lopez, A. C.; Torres, M. S.; García, N. G.; Mayedo, U. S.; Mendez-Rosado, L. A.
2020	The proresilients in multimodal programmes for the prevention of premature ageing	Rubikas, V.; Piatryshcha, T.; Rozhdestvenskaya, O.; Voronina, E.; Gerois, A.
2020	Single nucleotide polymorphisms in genes encoding xenobiotic metabolizing enzymes are associated with predisposition to arterial hypertension	Bushueva, O. Yu.
2020	Bioinformatic analysis of microduplications at 5p15.33: identification of TPPP as a candidate gene for autism and intellectual disability	Vasin, K. S.; Vorsanova, S. G.; Kurinnaia, O. S.; Shmitova, N. S.; Voinova, V. Y.
2020	Experience in managing a patient with a complicated course of SARS-CoV-2 infection: early pulmonary rehabilitation and prevention of pulmonary fibrosis : clinical case	Bontsevich, R. A.; Vovk, Y. R.; Adonina, A. V.; Solovyova, L. V.
2020	Screening Study for Anticonvulsive Activity of Lipophilic Fractions from Empetrum nigrum L.	Bezverkhniaia, E. A.; Poveteva, T. N.; Kadyrova, T. V.; Suslov, N. I.; Nesterova, Yu. V.