3pトリソミー
WordNet
- chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell
UpToDate Contents
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English Journal
- 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
- Rodovalho-Doriqui MJ1, Freitas PL, Pinho JD, Cavalli LR, Pereira SR.
- Genetics and molecular research : GMR.Genet Mol Res.2013 Jul 24;12(3):2562-6. doi: 10.4238/2013.July.24.7.
- We examined a girl presenting neuropsychomotor developmental delay and multiple malformations including antenatal and postnatal growth retardation, congenital heart defect, and facial dysmorphisms. Cytogenetic analysis was performed on peripheral blood lymphocytes with the GTG-banding technique, whi
- PMID 23979887
- Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization.
- Chen CP1, Chen YY, Chern SR, Wu PS, Su JW, Chen WL, Wang W.
- Taiwanese journal of obstetrics & gynecology.Taiwan J Obstet Gynecol.2013 Jun;52(2):278-84. doi: 10.1016/j.tjog.2013.04.023.
- OBJECTIVE: This study is aimed at prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism, and providing evidence for the limitation of array comparative genomic hybridization (aCGH) on placental tissues for molecular cytogene
- PMID 23915866
- Partial trisomy 3p and monosomy 5p diagnosed by spectral karyotyping (SKY).
- Imataka G, Tsuboi T, Kuribayashi R, Miyamoto K, Ichikawa G, Suzumura H, Arisaka O.
- Genetic counseling (Geneva, Switzerland).Genet Couns.2013;24(4):445-8.
- PMID 24551991
Japanese Journal
- Analysis of genomic alterations on urological malignancies by fluorescence in situ hybridization
- Matsuyama Hideyasu,Pan Yi,Oba Kazuo,Tsukamoto Manabu,Nagao Kazuhiro,Yamaguchi Shiro,Fukunaga Koji,Matsuda Kenji,Yoshihiro Satoru,Li Chunde,Kudren David,Bergerheim Ulf S. R.,Ekman Peter,Naito Katsusuke
- The bulletin of the Yamaguchi Medical School 50(1-4), 11-18, 2003-12
- … The following results had been obtained and published in the literature: Bradder cancer: Numericalalterations on chromosome 7, 9, and 17 by dual-color fruorescence in situ hybridization (FISH) demonstrated that chromosome 7 trisomy and 9 monosomy were the most frequently occurred not only in the tumor, but also in the surrounding intact bladder mucosa, and that 9 monosomy detected by using negative cytology specimen could predict early recurrence of superficial bladder cancer. …
- NAID 120000864659
- 術後5日間の酸素投与を必要とした3pトリソミー患者の全身麻酔
- 田中 利加子,野口 いづみ,高野 宏二,笹尾 真美,関田 俊介
- 日本歯科麻酔学会雑誌 31(2), 175-180, 2003-04-15
- NAID 10010769727
- 野口 いづみ,矢崎 素子,余 徳雄,高野 宏二,笹尾 真美,雨宮 義弘
- 障害者歯科 = JOURNAL OF THE JAPANESE SOIETY FOR DISABILITY AND ORAL HEALTH 19, 304, 1998-08-31
- NAID 10016501854
Related Links
- Duplication of the short arm of chromosome 3 with severe delay in mental development, craniofacial dysmorphism, urogenital maldevelopment, and various occasional anomalies, including cardiac defects, cleft lip and palate ...
- Partial trisomy 3p results from either unbalanced translocation or de novo duplication. Common clinical features consist of dysmorphic facial features, congenital heart defects, psychomotor and mental retardation ...