Nofmu.ru

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Host Informations
Host namesrv22.host-food.ru
IP address91.227.16.22
Location Russia
Latitude55.7386
Longitude37.6068
TimezoneEurope/Moscow
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Port Scanner (IP: 91.227.16.22)
 › Ftp: 21
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 › Telnet: 23
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 › Dns: 53
 › Http: 80
 › Pop3: 110
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nofmu-ykt.ru - Worth and traffic estimation | НОФМУ

Nofmu-ykt.ru was launched at August 8, 2013 and is 8 years and 251 days. It reaches roughly 30 users and delivers about 30 pageviews each month. Its estimated monthly revenue is $0.00.We estimate the value of nofmu-ykt.ru to be around $10.00.The domain nofmu-ykt.ru uses a Russia suffix and its server(s) are located in Russia with the IP number 178.208.83.43. nofmu-ykt.ru …

Statshow.com

DA: 16 PA: 17 MOZ Rank: 33

ЛОГ Гранты и конференции

Институт Мерзлотоведения СО РАН ИМЗ СО РАН Melnikov Permafrost Institute

Mpi.ysn.ru

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Paysafecard Code Generator Free Download

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news.un.org

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RT" C,\XNS(2=*]TRX0@J8c[X_.97+:C0913A3EN?G?BH?PRRNQTNOIL`[UYOV>Cq・SSUGIx、GKh]`cj儡J~olxML,?(KS9=47U:pr[YTZcS z諏 祝pnnョ赴、btSXイエj軍[NL楡JfZP]\{扼 ...

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Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in …

Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause of hearing impairment (HI). More than 300 allelic variants have been identified in the GJB2 gene. Spectrum and allelic frequencies of the GJB2 gene vary significantly among different ethnic groups worldwide. Until now, the spectrum and frequency of the pathogenic variants in …

Journals.plos.org

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Full text of "Jets and flashes" - Internet Archive

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Archive.org

DA: 11 PA: 50 MOZ Rank: 87

(PDF) Spectrum and Frequency of the GJB2 Gene Pathogenic …

Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause of hearing impairment (HI). More than 300 allelic variants have been identified in …

Researchgate.net

DA: 20 PA: 50 MOZ Rank: 41

Abstracts from the 50th European Society of Human Genetics …

M. N. Somuncu 1, A. G. Zamani 1, E. Goktas 1, A. Acar 2, M. S. Yıldırım 1. 1 Department of Medical Genetics, Meram Medical Faculty,Necmettin Erbakan University ...

Ncbi.nlm.nih.gov

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See other formats - Internet Archive

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(PDF) Reconstruction of SNP haplotypes with mutation c

** e-mail: [email protected] Received Septe mber 1, 2016; in final form, February 6, 201 7 Abstrac t ⎯ The c.-23+1G>A splice site mutation is one of the most frequent mutations of ge n e GJB2 (Cx26,

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Разное — Страница №917 — DBurn.ru - Фото сайт

Фото. Новые работы; Фото для критики; Выбор редакции

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