L. Livshits

发表

Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations

S. Popova, L. Tarskaya, P. Slominsky, 2001, European Journal of Human Genetics.

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

X. Estivill, J. Zieleński, T. Dörk, 2000, Human Genetics.

The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation and Neuromuscular Pathology

N. Zelinska, L. Livshits, A. Shatillo, 2022, Cytology and Genetics.

Polymorphism of the ADRB2 gene as a factor of hereditary susceptibility to the development of asthma and response to salbutamol therapy

P. Tatarsky, L. Livshits, G. Volynets, 2019, PERINATOLOGIYA I PEDIATRIYA.