V. Vakharlovsky

发表

Allele frequencies and molecular diagnosis in haemophilia A and B patients from russia and from some Asian Republics of the former U.S.S.R.

A. Mikhailov, V. Baranov, T. Kuznetzova, 1994, Prenatal diagnosis.

Proportion of the GSTM 10/0 genotype in some Slavic populations and its correlation with cystic fibrosis and some multifactorial diseases

V. Baranov, R. Belotserkovskaya, J. Perriot, 1996, Human Genetics.

Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III

M. Rask-Andersen, H. Schiöth, A. Egorova, 2011, BMC Medical Genetics.

Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R.

A. Mikhailov, V. Baranov, T. Kuznetzova, 1992, Prenatal diagnosis.

X;Y translocation in a girl with short stature and some features of Turner's syndrome: cytogenetic and molecular studies.

A. Baranov, T. Kuznetzova, P. Malet, 1994, Journal of medical genetics.

cytogenetic and molecular studies . and some features of Turner ' s syndrome : X ; Y translocation in a girl with short stature

V. Baranov, A. Baranov, T. Kuznetzova, 2022 .

Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment

A. Kiselev, V. Baranov, A. Baranov, 2008, Russian Journal of Genetics.

Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia

O. Evgrafov, A. Mikhailov, V. Baranov, 1993, Prenatal diagnosis.