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FSHD1 Diagnosis in a Russian Population Using a qPCR-Based Approach.
Diagnostics (Basel). 2021 May 28;11(6):982. doi: 10.3390/diagnostics11060982.
Diagnostics (Basel). 2021.
PMID: 34071558
Free PMC article.
Genotype-phenotype correlations in FSHD.
Zernov N, Skoblov M.
Zernov N, et al.
BMC Med Genomics. 2019 Mar 13;12(Suppl 2):43. doi: 10.1186/s12920-019-0488-5.
BMC Med Genomics. 2019.
PMID: 30871534
Free PMC article.
Review.
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Mutations in gonadotropin-releasing hormone signaling pathway in two nIHH patients with successful pregnancy outcomes.
Zernov N, Skoblov M, Baranova A, Boyarsky K.
Zernov N, et al.
Reprod Biol Endocrinol. 2016 Aug 20;14(1):48. doi: 10.1186/s12958-016-0183-8.
Reprod Biol Endocrinol. 2016.
PMID: 27544332
Free PMC article.
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Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles.
Zernov NV, Skoblov MY, Marakhonov AV, Shimomura Y, Vasilyeva TA, Konovalov FA, Abrukova AV, Zinchenko RA.
Zernov NV, et al.
J Invest Dermatol. 2016 Jun;136(6):1097-1105. doi: 10.1016/j.jid.2016.01.037. Epub 2016 Feb 20.
J Invest Dermatol. 2016.
PMID: 26902920
Free article.
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[Clinical and genetic characteristics of facioscapulohumeral muscular dystrophy Landuzi-Dezherina type 1].
Dadali EL, Sharkova IV, Zernov NV, Rudenskaya GE, Skoblov MY.
Dadali EL, et al. Among authors: zernov nv.
Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(11):122-128. doi: 10.17116/jnevro2017117111122-128.
Zh Nevrol Psikhiatr Im S S Korsakova. 2017.
PMID: 29265097
Russian.
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Two novel COL6A3 mutations disrupt extracellular matrix formation and lead to myopathy from Ullrich congenital muscular dystrophy and Bethlem myopathy spectrum.
Marakhonov AV, Tabakov VY, Zernov NV, Dadali EL, Sharkova IV, Skoblov MY.
Marakhonov AV, et al. Among authors: zernov nv.
Gene. 2018 Sep 25;672:165-171. doi: 10.1016/j.gene.2018.06.026. Epub 2018 Jun 9.
Gene. 2018.
PMID: 29894794
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