- 非症候性の
WordNet
- used to express refusal or denial or disagreement etc or especially to emphasize a negative statement; "no, you are wrong"
- a negative; "his no was loud and clear"
- referring to the degree to which a certain quality is present; "he was no heavier than a child" (同)no more
- not in any degree or manner; not at all; "he is no better today"
- quantifier; used with either mass nouns or plural count nouns for indicating a complete or almost complete lack or zero quantity of; "we have no bananas"; "no eggs left and no money to buy any"; "have you no decency?"; "did it with no help"; "Ill get you there in no time"
- the fifth of the seven canonical hours; about 3 p.m.
PrepTutorEJDIC
- 《名詞の前に置いて》『一つも』(『一人も,少しも』)・・・『ない』 / 《補語につけて》『決して・・・でない』 / 《省略文で》・・・なし;・・・お断り / 《話》少ししか(あまり)・・・ない / (肯定の問いに対して)『いいえ』;(否定の問いに対して)はい,ええ / 《not, norの前に挿入して》『いや』,否 / 《形容詞の前に置その形容詞を否定して》…どころではない / 《比較級の前に置いて》ちっとも…でない,…と全く同じ / 《… or no の形で》…であってもなくても / 《驚き・困惑・不信などを表して》とんでもない / 《単数形で》『拒否』,「『いいえ』」という返事 / 《複数形で》反対[投]票
UpToDate Contents
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- 1. 小児における知的障害（精神遅滞）：定義、原因および診断 intellectual disability mental retardation in children definition causes and diagnosis
- 2. 単一遺伝子性疾患の非メンデル遺伝のパターン non mendelian inheritance patterns of monogenic diseases
- 3. 非小細胞肺癌の診断および病期分類 diagnosis and staging of non small cell lung cancer
- 4. 非ST上昇型急性冠症候群における抗血小板薬 antiplatelet agents in acute non st elevation acute coronary syndromes
- 5. 脳転移に対する全身療法 systemic therapy for brain metastases
English Journal
- Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.
- Yoong SY, Mavrogiannis LA, Wright J, Fairley L, Bennett CP, Charlton RS, Spencer N.SourceSt Luke's Hospital, Little Horton Lane, Bradford BD5 0NA, UK; soo.yoong@bradfordhospitals.nhs.uk.
- Archives of disease in childhood.Arch Dis Child.2011 Sep;96(9):798-803. Epub 2011 May 17.
- Objective To determine the clinical sensitivity of DFNB1 genetic testing (analysis of the connexin 26 gene GJB2) for non-syndromic sensorineural hearing loss (SNHL) in British Pakistani children and extend to a comparison with British White children and literature data. Design Retrospective cohort s
- PMID 21586435
- A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia.
- Mendoza-Fandino G, Gee J, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers R, Leal S, Allayee H, Patel P.SourceInstitute for Genetic Medicine Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry of USC, University of Southern California, Los Angeles, CA, USA Bioinformatics and Biological Computing Unit, Weizmann Institute of Science, Tel Aviv, Israel Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
- Clinical genetics.Clin Genet.2011 Sep;80(3):265-272. doi: 10.1111/j.1399-0004.2010.01529.x. Epub 2010 Sep 8.
- Mendoza-Fandino GA, Gee JM, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers RM, Leal SM, Allayee H, Patel PI. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Mutations in the transcription
- PMID 21443745
Japanese Journal
- Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China
- Sun Yi,Chen Jing,Sun Hanjun [他]
- Journal of human genetics 56(1), 64-70, 2011-01
- NAID 40017436396
- Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage
- Park Mi-Hyun,Park Hong-Joon,Kim Kwang-Joong,Woo Hae-Mi,Kim Hyung-Jin,Lee Jong-Young,Park Hyun-Young,Koo Soo Kyung
- Genes & Genetic Systems 86(2), 117-121, 2011
- … We conducted a genome-wide linkage analysis using high-density SNP markers in two Korean families (families coded SD-J and SR-167) with autosomal dominant non-syndromic hearing loss (ADNSHL). … However, using non-parametric linkage analysis, it was possible to obtain significant evidence for linkage at 10q22.1~q23.31 (LOD 1.79; …
- NAID 130000758289
Related Links
- Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Different types of nonsyndromic ...
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★リンクテーブル★
| リンク元 | 「nonsyndromic」「非症候性」 |
| 拡張検索 | 「non-syndromic deafness」「non-syndromic hearing loss」 |
| 関連記事 | 「n」「syndromic」「non」 |
「nonsyndromic」
- 非症候性の
「非症候性」
「non-syndromic deafness」
「non-syndromic hearing loss」
「n」
- n.
- pの前の[n]はmと記載する。synptom→symptom
「syndromic」
- adj.
- 症候性の
「non」
- comb form.
- 関
- un