Detalhe da pesquisa
1.
High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients.
BMC Genomics
; 23(1): 252, 2022 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35365085
2.
Gene pool preservation across time and space In Mongolian-speaking Oirats.
Eur J Hum Genet
; 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38605123
3.
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania.
PeerJ
; 11: e14514, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36743950
4.
Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation.
Front Genet
; 12: 678374, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34220950
5.
Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population.
Genes (Basel)
; 12(6)2021 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34071867
6.
Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner Asia.
Eur J Hum Genet
; 27(9): 1466-1474, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30976109