Genomic imprinting and its role in ethiology of human hereditary diseases by S. A. Nazarenko

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University students’ anticipated stigma toward individuals with hereditary chronic diseases in oman: a cross-sectional study by Ali Alkalbani, Maryam Alharrasi, Jansi Natarajan, Khaldoun Aldiabat, Ammar Al Badi, Amjad Al Rumhi, Khalid Alqassabi, Nawal Al Aamri, Omar Al Omari

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The clinical spectrum and prevalence of hereditary ophthalmopathology child population in 12 districts of the Rostov region by O. L. Kireeva, O. V. Chlebnikova, S. S. Amelina, G. I. Elchinova, R. A. Zinchenko, V. V. Kadsjyshev, E. K. Ginter

Subjects: “…the prevalence of hereditary diseases…”
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Norry's disease in a child: clinical case by T. A. Kryuchkova, E. V. Matvienko

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A causal assessment of blindness in schools for blind in southern Rajasthan by Hardik Kiri, Lipa Mohanty, Seemal Goyal

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Current Issues in Terminology and Classification of Hereditary Disorders at Endocrine Cancer by S. B. Pinsky, V. A. Beloborodov, V. V. Dvornichenko, Yu. K. Batoroev, V. A. Vorobev

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The results of the cross-sectional study of platelet aggregative function in children with hemorrhagic syndrome by Olga B. Gordeeva, Albina V. Dobrotok, Mariia V. Volkova, Natalia L. Aleshenko, Vladimir S. Kargin, Irine Dzharkava, Nadezhda F. Zhdanovskaia

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Duchenne Muscular Dystrophy: Modern Approaches in Patient Management by Inga V. Anisimova, Svetlana B. Artemyeva, Elena D. Belousova, Nato D. Vashakmadze, Dmitriy V. Vlodavets, Tatiana A. Gremyakova, Olga S. Groznova, Valentina I. Guzeva, Elena V. Gusakova, Lyudmila M. Kuzenkova, Alexey L. Kurenkov, Sergey I. Kutsev, Svetlana V. Mikhaylova, Lyudmila P. Nazarenko, Sergey S. Nikitin, Artem Yu. Novikov, Tatiana V. Podkletnova, Elena V. Polevichenko, Alexander V. Polyakov, Gennady G. Prokopyev, Dmitry I. Rudenko, Svetlana A. Repina, Evgeniia V. Romanenko, Sergey O. Ryabykh, Gul’zhan E. Sakbaeva, Elena Yu. Sapego, Liliia R. Selimzyanova, Andrey A. Stepanov, Dmitry M. Subbotin, Vasiliy M. Suslov, Elena V. Tozliyan, Dmirty A. Feklistov, Nadezhda I. Shakhovskaya, Ekaterina V. Shreder

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Value of medical genetic consultation at digestive organs diseases by T. V. Filippova

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Familial Mediterranean fever (a periodic disease): The present-day view of the problem by Evgeny Stanislavovich Fedorov, S O Salugina, N N Kuzmina

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Ocular symptoms of Saul — Wilson syndrome in children by L. V. Kogoleva, T. N. Vorontsova, Ju. A. Bobrovskaya

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Biosample collection in a biobank to solve problems of personalized medicine by O. V. Kopylova, A. I. Ershova, A. N. Meshkov, M. S. Pokrovskaya, I. A. Efimova, A. S. Limonova, A. V. Blokhina, Z. Z. Serebryanskaya, S. A. Smetnev, V. I. Mikhailina, R. P. Myasnikov, A. V. Kiseleva, E. V. Garbuzova, V. A. Metelskaya, A. L. Borisova, O. M. Drapkina

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Adenoviral Vectors for Gene Therapy of Hereditary Diseases by Anna Muravyeva, Svetlana Smirnikhina

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A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis t... by N. V. Komissarova, A. A. Malkova, O. P. Potorochina, A. A. Ovchinnikova, P. O. Ivanina, D. O. Bayusheva

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The knowledge, attitudes and practices regarding family history of hereditary diseases amongst undergraduate students at the University of the Free State by Lynette J. van der Merwe, Gaby Nel, Caitlin Williams, Swalica Erasmus, Riana Nel, Marize Kolver, Benine van den Heever, Gina Joubert

Subjects: “…hereditary diseases…”
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Management of biobanking for medical genetics research by V. Yu. Tabakov

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An artifiсial intelligence computer system for differential diagnosis of lysosomal storage diseases by B. A. Kobrinskii, N. A. Blagosklonov, N. S. Demikova, E. A. Nikolaeva, Y. Y. Kotalevskaya, L. P. Melikyan, Y. M. Zinovieva

Subjects: “…hereditary diseases…”
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EPILEPSY IN 11 PATIENTS WITH TYPICAL RETT SYNDROME CAUSED BY MECP2 MUTATION: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS, COURSE, THERAPY (RESULTS OF THE AUTHORS’ OBSERVAT... by M. Yu. Bobylova, K. Yu. Mukhin, I. V. Ivanova, I. V. Nekrasova, O. A. Pylaeva, N. Yu. Borovikova, E. S. Il’ina

Subjects: “…hereditary diseases in children…”
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On the Prospects for Child Disability Prevention Research by Alexander A. Baranov, Rimma N. Terleckaya

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Molecular-genetic study of <i>SMN1</i> and <i>SMN2</i> genes associated with spinal muscular atrophy in individuals with infertility prior to in vitro fertilization by E. V. Kudryavtseva, O. V. Lagutina, V. V. Kovalev, S. S. Deryabina, I. A. Zakharova, A. Yu. Cherepennikova

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