112 related articles for article (PubMed ID: 17987598)
1. Amniotic fluid with an inconclusive result by interphase FISH and 45,X by routine G-banding turned out to have 46,X,+ mar.ish der(X)(DXZ1+).
Xu J; Mak L; Jung J
Prenat Diagn; 2007 Dec; 27(13):1258-9. PubMed ID: 17987598
[No Abstract] [Full Text] [Related]
2. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
[TBL] [Abstract][Full Text] [Related]
3. Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.
Chen CP; Chang TY; Chern SR; Town DD; Pan CW; Lee MS; Wang W
Prenat Diagn; 2003 Apr; 23(4):352-3. PubMed ID: 12673645
[No Abstract] [Full Text] [Related]
4. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
Liang Y; Luo XP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
5. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
6. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
7. [Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].
Wen J; Liang D; Liao X; Xue J; Tang G; Xia Y; Long Z; Dai H; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):659-63. PubMed ID: 19953489
[TBL] [Abstract][Full Text] [Related]
8. A fetus with a 90,XX karyotype.
Sánchez JM; Dubner M; de Diaz SL; Vilaseco G
Prenat Diagn; 1999 Feb; 19(2):178-9. PubMed ID: 10215079
[No Abstract] [Full Text] [Related]
9. Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul D; Attanasio L; Oehler E; Hamosh A; Blakemore K; Stetten G
Prenat Diagn; 2007 Apr; 27(4):373-9. PubMed ID: 17286317
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.
Zhang L; Ren M; Song G; Zhang Y; Liu X; Zhang X; Wang J
Mol Med Rep; 2018 Feb; 17(2):2811-2816. PubMed ID: 29257243
[TBL] [Abstract][Full Text] [Related]
11. Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism.
Su SY; Chueh HY; Li CP; Chang YL; Chang SD; Chen CP
Taiwan J Obstet Gynecol; 2015 Oct; 54(5):588-91. PubMed ID: 26522116
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
Xiao HM; Tan YQ; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
[TBL] [Abstract][Full Text] [Related]
13. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report.
Chang SD; Lin SL; Chen FP; Chu KK
J Reprod Med; 1996 Mar; 41(3):175-8. PubMed ID: 8778416
[TBL] [Abstract][Full Text] [Related]
14. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
[TBL] [Abstract][Full Text] [Related]
15. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
Palka C; Alfonsi M; Morizio E; Soranno A; La Rovere D; Matarrelli B; Rullo AL; Zori R; Chiarelli F; Calabrese G
Eur J Med Genet; 2011; 54(3):333-6. PubMed ID: 21354345
[TBL] [Abstract][Full Text] [Related]
16. Amniotic fluid interphase fluorescence in situ hybridization (FISH) for detection of aneuploidy; experiences in 130 prenatal cases.
Lim HJ; Kim YJ; Yang JH; Kim EJ; Choi JS; Jung SH; Ahn HK; Han JY; Kim MY; Choi KH; Kim JM; Kim YM; Park SY; Ryu HM
J Korean Med Sci; 2002 Oct; 17(5):589-92. PubMed ID: 12378006
[TBL] [Abstract][Full Text] [Related]
17. Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH.
Tsuchiya K; Schueler MG; Dev VG
Prenat Diagn; 2001 Oct; 21(10):852-5. PubMed ID: 11746128
[TBL] [Abstract][Full Text] [Related]
18. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
Huang Y; Sun X; Li Q
Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
[TBL] [Abstract][Full Text] [Related]
19. Role of multicolor fluorescence in situ hybridization (FISH) in simultaneous detection of probe sets for chromosome 18, X and Y in uncultured amniotic fluid cells.
Kim JI; Rhee JH
J Korean Med Sci; 1999 Aug; 14(4):438-42. PubMed ID: 10485625
[TBL] [Abstract][Full Text] [Related]
20. Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma.
Vičić A; Zudenigo D; Korać P; Liehr T; Stipoljev F
Gene; 2013 Nov; 531(1):90-1. PubMed ID: 23999188
[No Abstract] [Full Text] [Related]
[Next] [New Search]