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Results of search for 'au:"Kurtanov, Kh A"'
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Authors
Alekseeva, E I
Gurinova, E E
Ikeuchi, T
Korotkov, M N
Kurtanov, Kh A
Maksimova, N R
Marusin, A V
Nikolaeva, I A
Nishizava, M
Nogovicina, A N
Nogovitsyna, A N
Onodera, O
Puzyrev, V P
Stepanov, V A
Stepanova, S K
Sukhomiasova, A L
Svarovskaya, M G
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Topics
Abnormalities, Multiple
Adult
Aged
Alleles
Catchment Area, Health
Exons
Female
Founder Effect
Gene Frequency
Haplotypes
Heterozygote
Humans
Inuit
Male
Middle Aged
Muscular Dystrophy, Oculopharyngeal
Neoplasm Proteins
Point Mutation
Siberia
genetics
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Languages
Russian
Your search returned 3 results.
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1.
[Population frequency and age of mutation G5741→A in gene NBAS which is a cause of SOPH syndrome in Sakha (Yakutia) Republic].
[electronic resource]
by
Maksimova, N R
Nogovicina, A N
Kurtanov, Kh A
Alekseeva, E I
Producer:
20180205
In:
Genetika
vol. 52
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2.
[Haplotype Analysis of Oculopharyngeal Muscular Dystrophy (OPMD) Locus in Yakutia].
[electronic resource]
by
Marusin, A V
Kurtanov, Kh A
Maksimova, N R
Svarovskaya, M G
Stepanov, V A
Producer:
20160923
In:
Genetika
vol. 52
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3.
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)].
[electronic resource]
by
Maksimova, N R
Nikolaeva, I A
Korotkov, M N
Ikeuchi, T
Onodera, O
Nishizava, M
Stepanova, S K
Kurtanov, Kh A
Sukhomiasova, A L
Nogovitsyna, A N
Gurinova, E E
Stepanov, V A
Puzyrev, V P
Producer:
20081112
In:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
vol. 108
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