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	21.	Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes. [electronic resource] by Markova, T G Brazhkina, N B Bliznech, E A Bakhshinyan, V V Polyakov, A V Tavartkiladze, G A Producer: 20160920 In: International journal of pediatric otorhinolaryngology vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	[Endoscope-assisted keyhole approach in cerebral aneurysm surgery]. [electronic resource] by Dzhindzhikhadze, R S Dreval', O N Lazarev, V A Polyakov, A V Kambiev, R L Davudov, A M Producer: 20190226 In: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Novosibirsk revisited 24 years on: chromosome polymorphism in the Novosibirsk population of the common shrew Sorex araneus L. [electronic resource] by Polyakov, A V Chadova, N B Rodionova, M I Panov, V V Dobrotvorsky, A K Searle, J B Borodin, P M Producer: 19971009 In: Heredity vol. 79 ( Pt 2) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	A new genetic variant of mdx mice: study of the phenotype. [electronic resource] by Krivov, L I Stenina, M A Yarygin, V N Polyakov, A V Savchuk, V I Obrubov, S A Komarova, N V Producer: 20100120 In: Bulletin of experimental biology and medicine vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients. [electronic resource] by Shchagina, O A Milovidova, T B Murtazina, A F Rudenskaya, G E Nikitin, S S Dadali, E L Polyakov, A V Producer: 20201007 In: Molecular biology reports vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Peculiarities of Pharmacokinetics and Bioavailability of Some Cardiovascular Drugs under Conditions of Antiorthostatic Hypokinesia. [electronic resource] by Polyakov, A V Svistunov, A A Kondratenko, S N Kovachevich, I V Repenkova, L G Savelyeva, M I Kukes, V G Producer: 20210201 In: Bulletin of experimental biology and medicine vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Laminopathies in Russian families. [electronic resource] by Rudenskaya, G E Polyakov, A V Tverskaya, S M Zaklyazminskaya, E V Chukhrova, A L Groznova, O E Ginter, E K Producer: 20081111 In: Clinical genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Hidden X chromosomal mosaicism in a 46,XX male. [electronic resource] by Chernykh, V B Kurilo, L F Shilova, N V Zolotukhina, T V Ryzhkova, O P Bliznetz, E A Polyakov, A V Producer: 20100121 In: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene. [electronic resource] by Mersiyanova, I V Perepelov, A V Polyakov, A V Sitnikov, V F Dadali, E L Oparin, R B Petrin, A N Evgrafov, O V Producer: 20000807 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Unique mosaic X/Y translocation/insertion in infant 45,X male. [electronic resource] by Chernykh, V B Vyatkina, S V Antonenko, V G Shilova, N V Zolotukhina, T V Kurilo, L F Chukhrova, A L Polyakov, A V Producer: 20090121 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	In vitro and in vivo studies on nanocrystalline Ti fabricated by equal channel angular pressing with microcrystalline CP Ti as control. [electronic resource] by Nie, F L Zheng, Y F Wei, S C Wang, D S Yu, Z T Salimgareeva, G K Polyakov, A V Valiev, R Z Producer: 20131022 In: Journal of biomedical materials research. Part A vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]. [electronic resource] by Mironovich, O L Bliznetz, E A Markova, T G Geptner, E N Lalayants, M R Zelikovich, E I Tavartkiladze, G A Polyakov, A V Producer: 20180216 In: Genetika vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	33.	[Epidemiology of hearing loss in children of the first year of life]. [electronic resource] by Chibisova, S S Markova, T G Alekseeva, N N Yasinskaya, A A Tsygankova, E R Bliznetz, E A Polyakov, A V Tavartkiladze, G A Producer: 20190115 In: Vestnik otorinolaringologii vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	[The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.] [electronic resource] by Simakova, T S Bragin, A G Glushkova, M A Petrova, N V Polyakov, A V Kondratieva, E I Sherman, V D Pavlov, A E Publication details: Klinicheskaia laboratornaia diagnostika 2017 In: Klinicheskaia laboratornaia diagnostika vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21. [electronic resource] by Ismailov, S M Fedotov, V P Dadali, E L Polyakov, A V Van Broeckhoven, C Ivanov, V I De Jonghe, P Timmerman, V Evgrafov, O V Producer: 20010920 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	[The clinical definition and etiology of Pendred syndrome (a review of the literature and clinical observations)]. [electronic resource] by Markova, T G Geptner, E N Lalayants, M R Zelikovich, E I Chugunova, T I Mironovich, O L Bliznetz, E A Polyakov, A V Tavartkiladze, G A Producer: 20170614 In: Vestnik otorinolaringologii vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients. [electronic resource] by Mersiyanova, I V Ismailov, S M Polyakov, A V Dadali, E L Fedotov, V P Nelis, E Löfgren, A Timmerman, V van Broeckhoven, C Evgrafov, O V Producer: 20000516 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	X-linked hypohidrotic ectodermal dysplasia: clinical and molecular genetic analysis of a large Russian family with a synonymous p.Ser267= (c.801A>G) splice site mutation. [electronic resource] by Milovidova, T B Schagina, O A Freire, M V Demina, N A Filatova, A Y Skoblov, M Y Stepanova, A A Chuhrova, A L Polyakov, A V Producer: 20200708 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	[The results of cochlear implantation in the patient with hereditary and non-hereditary hearing loss]. [electronic resource] by Tavartkiladze, G A Bakhshinyan, V V Markova, T G Tsygankova, E R Petrova, I P Goykhburg, M V Chibisova, S S Bliznetz, E A Polyakov, A V Producer: 20170614 In: Vestnik otorinolaringologii vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia. [electronic resource] by Baranov, V S Gorbunova, V N Malysheva, O V Artemyeva, O V Kascheeva, T K Evgrafov, O V Polyakov, A V Lebedev, V M Kuznetzova, T V Shlykova, S N Producer: 19930831 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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