Vol. 58, No. 10, 2022
“Mendelian Code” in the Genetic Structure of Common Multifactorial Diseases
p. 1159 abstract
Interloci CNV Interactions in Variability of the Phenotypes of Neurodevelopmental Disorders
p. 1169 abstract
Pleiotropy of Copy Number Variation in Human Genome
p. 1180 abstract
X-Linked CNV in Pathogenetics of Intellectual Disability
p. 1193 abstract
The Role of Splicing in the Pathogenesis of Monogenic Diseases
p. 1208 abstract
Clinical and Genetic Characteristics of Congenital Long QT Syndrome
p. 1216 abstract
Genetic Interrelation of the Chulym Turks with Khakass and Kets according to Autosomal SNP Data and Y-Chromosome Haplogroups
p. 1228 abstract
ADAMTS1 Is Differentially Expressed in Human Lymphocytes with Various Frequencies of Endogenous γH2AX Foci and Radiation-Induced Micronuclei
p. 1235 abstract
Genetic Structure of Susceptibility to Cardiovascular Continuum Comorbidity
p. 1245 abstract
Alternative Splicing Landscape of Placental Decidual Cells during Physiological Pregnancy
p. 1257 abstract
Association between Ca2+ Signaling Pathway-Related Gene Polymorphism and Age-Related Hearing Loss in Qingdao Chinese Elderly
p. 1266 abstract