出典: meddic

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/06/01 08:23:08」(JST)

wiki ja

[Wiki ja表示]

wiki en

[Wiki en表示]

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.


  • Craniosynostosis, psychomotor retardation, and facial dysmorphic features in a Spanish patient with a 4q27q28.3 deletion.
  • Fernández-Jaén A1, Fernández-Perrone AL, Fernández-Mayoralas DM, Calleja-Pérez B, Sánchez-Hombre Mdel C, Fernández EC, López-Martín S.
  • Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery.Childs Nerv Syst.2014 Dec;30(12):2157-61. doi: 10.1007/s00381-014-2474-8. Epub 2014 Jul 1.
  • CASE REPORT: We describe an unusual clinical case with an 11-Mb deletion at 4q27 (chr4: 123094652-134164491), craniosynostosis (CS), mild psychomotor retardation, and facial dysmorphic features. This deletion involves 18 genes; FGF2, NUDT6, and SPRY1 are primarily or secondarily implicated in human
  • PMID 24980605
  • Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion.
  • Campbell CL1, Collins RT 2nd, Zarate YA.
  • Birth defects research. Part A, Clinical and molecular teratology.Birth Defects Res A Clin Mol Teratol.2014 Nov 7. doi: 10.1002/bdra.23324. [Epub ahead of print]
  • BACKGROUND: Kleefstra syndrome arises from haploinsufficiency of EHMT1 caused by either microdeletions at 9q34.3 or intragenic mutations. Patients with Kleefstra syndrome have multisystem involvement including intellectual disability, hypotonia, and characteristic facial features.METHODS: We report
  • PMID 25380126
  • Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
  • Pires R, Pires LM, Vaz SO, Maciel P, Anjos R, Moniz R, Branco CC, Cabral R, Carreira IM, Mota-Vieira L.
  • BMC genetics.BMC Genet.2014 Nov 7;15(1):115. [Epub ahead of print]
  • BackgroundThe rearrangements in the 22q11.2 chromosomal region, responsible for the 22q11.2 deletion and microduplication syndromes, are frequently associated with congenital heart disease (CHD). The present work aimed to identify the genetic basis of CHD in 87 patients from the São Miguel Island,
  • PMID 25376777


  • Epileptic spasmsを呈したMECP2領域微細重複症候群の一例
  • 衞藤 薫/坂内 優子/島田 姿野/大谷 ゆい/塩田 睦記/石垣 景子/下島 圭子/山本 俊至/小國 弘量/大澤 眞木子
  • 東京女子医科大学雑誌 83(E1), E250-E254, 2013-01-31
  • … 同年当院を受診し、アレイCGHにて上記診断した。 …
  • NAID 110009559411
  • アレイCGHを用いたDMD遺伝子の重複変異領域の断端解析
  • 齊藤 崇/石垣 景子/村上 てるみ/佐藤 孝俊/梶野 幸子/武田 伸一/大澤 真木子
  • 東京女子医科大学雑誌 83(E1), E20-E24, 2013-01-31
  • … 我々は重複変異における断端解析を簡易化するために、DMD遺伝子全領域をカバーするアレイCGH(DMD-aCGH)の有用性を検討した。 …
  • NAID 110009559372
  • Computer-generated holograms using multiview images captured by a small number of sparsely arranged cameras
  • Ohsawa Yusuke,Yamaguchi Kazuhiro,Ichikawa Tsubasa,Sakamoto Yuji
  • Applied Optics 52(1), A167-A176, 2013-01-01
  • … In this paper, we propose a method to improve CGH using MVIs that obtains the MVIs by using voxel models rather than cameras. …
  • NAID 120005228224


Comparative Genomic Hybridization (CGH)法は、全染色体を対象にしてゲノムDNAの過剰、欠失、増幅などのコピー数異常を短時間で検出する方法である。Joe Gray, Dan Pinkel, O-P Kallioniemiらによって開発された技術であり、その成果 ...
Clinical Gastroenterology and Hepatology (CGH) provides readers with a broad spectrum of themes in gastroenterology and hepatology, including the diagnostic, endoscopic, interventional, and therapeutic advances in cancer ...


 Übersicht zur Durchführung der Array-CGH Darstellung der Array-CGH-TechnikcghRat Genome CGH array 2 x 105kDescription Array-CGH protocol.svgFigure 2.

リンク元比較ゲノムハイブリダイゼーション法」「比較ゲノムハイブリダイゼーション」「comparative genomic hybridization
拡張検索CGHマイクロアレイ法」「array CGH」「CGH法



comparative genomic hybridization technique, comparative genomic hybridization method
comparative genomic hybridization法, CGH法
比較ゲノムハイブリダイゼーション, CGH
[show details]



comparative genomic hybridizationCGH
[show details]

comparative genomic hybridization」

  [★] 比較ゲノムハイブリダイゼーション CGH


  [★] 比較ゲノムハイブリダイゼーションマイクロアレイ法

array CGH」

  [★] アレイ比較ゲノムハイブリダイゼーション


  [★] 比較ゲノムハイブリダイゼーション法



WordNet   license wordnet

「the 3rd letter of the Roman alphabet」

WordNet   license wordnet

「(music) the keynote of the scale of C major」

WordNet   license wordnet

「a general-purpose programing language closely associated with the UNIX operating system」

PrepTutorEJDIC   license prepejdic


"" より作成