Petrin AN - Search Results

1

Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35.

Rogaev EI, Rogaeva EA, Korovaitseva GI, Farrer LA, Petrin AN, Keryanov SA, Turaeva S, Chumakov I, St George-Hyslop P, Ginter EK. Rogaev EI, et al. Among authors: petrin an. Hum Mol Genet. 1996 May;5(5):699-703. doi: 10.1093/hmg/5.5.699. Hum Mol Genet. 1996. PMID: 8733140

2

[An attempt to locate the gene for congenital cataracts using linkage analysis].

Ginter EK, Petrin AN, Spitsyn VA, Rogaev EI. Ginter EK, et al. Among authors: petrin an. Genetika. 1991 Oct;27(10):1840-9. Genetika. 1991. PMID: 1778455 Russian.

3

Emery-Dreifuss syndrome: genetic and clinical varieties.

Rudenskaya GE, Ginter EK, Petrin AN, Djomina NA. Rudenskaya GE, et al. Among authors: petrin an. Am J Med Genet. 1994 Apr 15;50(3):228-33. doi: 10.1002/ajmg.1320500304. Am J Med Genet. 1994. PMID: 8042665

4

[Further analysis of location of the gene for inborn dominant Nochurli cataract].

Ginter EK, Rogaev EI, Korovaĭtseva GI, Turaeva ShM, Petrin AN, Spitsyn VA, Tarlycheva LV. Ginter EK, et al. Among authors: petrin an. Genetika. 1993 Apr;29(4):670-4. Genetika. 1993. PMID: 8354473 Russian.

5

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.

Mersiyanova IV, Perepelov AV, Polyakov AV, Sitnikov VF, Dadali EL, Oparin RB, Petrin AN, Evgrafov OV. Mersiyanova IV, et al. Among authors: petrin an. Am J Hum Genet. 2000 Jul;67(1):37-46. doi: 10.1086/302962. Epub 2000 Jun 7. Am J Hum Genet. 2000. PMID: 10841809 Free PMC article.

6

[Medical genetic study of the population of Kostroma Province. V. The hereditary pathology burden of urban and rural populations].

Petrin AN, Ginter EK, Khisamova MV. Petrin AN, et al. Genetika. 1988 Jan;24(1):151-5. Genetika. 1988. PMID: 2965662 Russian.

7

[Prevalence of hereditary pathologies in residents of the Kirov Province].

Mamedova RA, Ginter EK, Petrin AN, Khvatova AV, Khlebnikova OV, Kadoshnikova MIu, Mikhaĭlova LK, Prokhorov AIu, Rudenskaia GE, Lukashova ID, et al. Mamedova RA, et al. Among authors: petrin an. Genetika. 1992 Apr;28(4):186-91. Genetika. 1992. PMID: 1386329 Russian.

8

[Population genetic study of hereditary motor and sensory neuropathy in the Kirov region].

Rudenskaia GE, Ginter EK, Mamedova RA, Petrin AN, Poleshchuk VV. Rudenskaia GE, et al. Among authors: petrin an. Genetika. 1993 Nov;29(11):1878-88. Genetika. 1993. PMID: 8307375 Russian.

9

[Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region].

Ginter EK, Budagova KA, Revazov AA, Petrin AN, Bugaeva EA. Ginter EK, et al. Among authors: petrin an. Genetika. 1986 Jul;22(7):1199-206. Genetika. 1986. PMID: 2943634 Russian.

10

[Medico-genetical study of the population of the Kostroma Region. IV. Genetic load and diversity of hereditary pathology in 5 districts].

Petrin AN, Ginter EK, Rudenskaia GE, Burkova LM, Khlebnikova OV. Petrin AN, et al. Genetika. 1987 Jul;23(7):1319-27. Genetika. 1987. PMID: 2958387 Russian.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

31 results

Search Page

Filters