- 二分の
WordNet
- divided into two lobes; "a bifid petal"
- divided into two portions almost to the base
- involving two parts or elements; "a bipartite document"; "a two-way treaty" (同)two-part, two-way
- cut in half or cut in two; "bisect a line"
- dividing into two equal parts
- divided or dividing into two sharply distinguished parts or classifications
PrepTutorEJDIC
- 2部［2通］から成る; 2者の;（葉が）二裂の
- …'を'2分する,2等分する
- 二つに分けること;2等分
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/09/17 05:34:11」(JST)
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- 1. 母斑性基底細胞癌症候群 nevoid basal cell carcinoma syndrome
- 2. アンドロゲン受容体障害の病因および臨床症状 pathogenesis and clinical manifestations of disorders of androgen action
- 3. 遺伝性皮膚症 the genodermatoses
- 4. 基底細胞癌の疫学および臨床的特徴 epidemiology and clinical features of basal cell carcinoma
- 5. 甲状腺の外科解剖学 surgical anatomy of the thyroid gland
English Journal
- Congenital malformations of the ureter: anatomical studies.
- Dorko F1, Tokarčík J2, Výborná E2.
- Anatomical science international.Anat Sci Int.2016 Jun;91(3):290-4. doi: 10.1007/s12565-015-0296-8. Epub 2015 Aug 19.
- The ureter is a derivate of the Wolffian mesonephric duct and undergoes complex changes during development. The most common developmental anomaly is complete duplication of the ureter. Duplication of the ureter may be complete or incomplete. Incomplete duplication of ureter is well known as bifid ur
- PMID 26286110
- [Loeys-Dietz syndrome (TGFβR2 mutation) in a 4-year-old child with thoracic aortic aneurysm].
- De Potter MJ1, Edouard T2, Amadieu R1, Plaisancié J3, Julia S3, Hadeed K1, Hascoët S1, Acar P1, Dulac Y4.
- Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie.Arch Pediatr.2016 May;23(5):504-7. doi: 10.1016/j.arcped.2016.02.001. Epub 2016 Mar 24.
- Loeys-Dietz syndrome is a rare form of connective tissue disorder, whose clinical features can resemble those of Marfan syndrome, but with a more unpolished appearance. Recently brought out, this pathology remains little known; however, its consequences may be dramatic. We report on the case of a 4-
- PMID 27017362
- A Novel Mutation In Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome In A Patient Presenting With Gynecomastia At Puberty.
- Koçyiğit C, Sarıtaş S, Çatlı G, Onay H, Dündar BN.
- Journal of clinical research in pediatric endocrinology.J Clin Res Pediatr Endocrinol.2016 Apr 18. doi: 10.4274/jcrpe.2637. [Epub ahead of print]
- BACKGROUND: Partial androgen insensitivity syndrome (PAIS) typically presents with micropenis, perineoscrotal hypospadias, and a bifid scrotum with descending or undescending testes and gynecomastia at puberty. It is an X-linked recessive disorder resulting from mutations in androgen receptor (AR) g
- PMID 27087292
Japanese Journal
- A Case of Cutaneous Meningioma in the Rudimentary Meningocele
- Hiroshima Journal of Medical Sciences 65(1), 9-12, 2016-03
- NAID 120005743716
- ナンセンス変異による<i>PTCH1</i>遺伝子を伴った母斑基底細胞症候群の1例
- 日本口腔外科学会雑誌 61(2), 120-124, 2015
- NAID 130005099058
- Loeys-Dietz 症候群
- 日本小児循環器学会雑誌 30(3), 232-238, 2014
- NAID 130004879018
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Related Pictures
★リンクテーブル★
| リンク元 | 「bipartite」「二分」「bisect」「bisection」「dichotomous」 |
| 拡張検索 | 「open spina bifida」 |
「bipartite」
- 二連の、二分の
「二分」
「bisect」
- 二分する
「bisection」
「dichotomous」
- 二分の