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Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.
Science. 2006 Nov 10;314(5801):982-5. doi: 10.1126/science.1133276.
Science. 2006.
PMID: 17095700
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.
Bliznetz EA, Tverskaya SM, Zinchenko RA, Abrukova AV, Savaskina EN, Nikulin MV, Kirillov AG, Ginter EK, Polyakov AV.
Bliznetz EA, et al. Among authors: abrukova av.
Eur J Hum Genet. 2009 May;17(5):664-72. doi: 10.1038/ejhg.2008.234. Epub 2009 Jan 28.
Eur J Hum Genet. 2009.
PMID: 19172990
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. Among authors: abrukova av.
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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[Analysis of reproductive parameters of urban and rural population of Chuvashia].
El'chinova GI, Zinchenko PA, Kirillov AG, Abrukova AV.
El'chinova GI, et al. Among authors: abrukova av.
Genetika. 2005 Jun;41(6):850-4.
Genetika. 2005.
PMID: 16080612
Russian.
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Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population.
Petrova NV, Marakhonov AV, Balinova NV, Abrukova AV, Konovalov FA, Kutsev SI, Zinchenko RA.
Petrova NV, et al. Among authors: abrukova av.
Genes (Basel). 2021 May 27;12(6):820. doi: 10.3390/genes12060820.
Genes (Basel). 2021.
PMID: 34071867
Free PMC article.
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[Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes].
Stepanova AA, Abrukova AV, Savaskina EN, Poliakov AV.
Stepanova AA, et al. Among authors: abrukova av.
Genetika. 2012 Jul;48(7):863-71.
Genetika. 2012.
PMID: 22988772
Russian.
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