V. N. Gorbunova

发表

Chromosomal localization of ceruoplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes

V. Baranov, N. Rubtsov, N. Timchenko, 2004, Chromosoma.

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.

Genetics and epigenetics of syntropic diseases

V. N. Gorbunova, 2010, Russian Journal of Genetics: Applied Research.

Comparative analysis of deletion F508 frequency in fibrosis patients

V. Baranov, L. Livshitz, T. Ivaschenko, 1991 .

RELP analysis and screening of deletions in the families of patients with DMD

V. Baranov, O. Malysheva, V. N. Gorbunova, 1991 .

Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR

V. Kalinin, V. Baranov, L. Livshitz, 2005, Human Genetics.

RFLP analysis of Duchenne muscular dystrophy gene in population of Leningrad and in high risk families

M. Aseev, V. N. Gorbunova, V. Krasilnikov, 1990 .

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

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

[Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy].

V. Baranov, O. Malysheva, V. V. Krasil’nikov, 1991, Molekuliarnaia genetika, mikrobiologiia i virusologiia.

[High frequency of spontaneous occurrence of mutations affecting viability in chromosome 2 of Drosophila melanogaster line "HA"].

V. N. Gorbunova, L. Kaidanov, 1975, Genetika.