228 related articles for article (PubMed ID: 15712342)
1. Mosaic trisomy (8)(p22 --> pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences.
de Pater JM; Kroes HY; Verschuren M; van Oppen AC; Albrechts JC; Engelen JJ
Prenat Diagn; 2005 Feb; 25(2):151-5. PubMed ID: 15712342
[TBL] [Abstract][Full Text] [Related]
2. Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.
de Pater J; Van der Sijs-Bos C; Prins M; Derks J; Albrechts J; Engelen J
Eur J Med Genet; 2006; 49(4):306-12. PubMed ID: 16461028
[TBL] [Abstract][Full Text] [Related]
3. Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
de Pater JM; Govaerts LC; de Man SA; van der Sijs-Bos CJ; Christiaens GC; van Dam WM; Loneus WH; Engelen JJ
Prenat Diagn; 2003 Sep; 23(9):747-51. PubMed ID: 12975787
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
Starke H; Schreyer I; Kähler C; Fiedler W; Beensen V; Heller A; Nietzel A; Claussen U; Liehr T
Prenat Diagn; 1999 Dec; 19(12):1169-74. PubMed ID: 10590438
[TBL] [Abstract][Full Text] [Related]
7. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
9. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Chen CP; Su YN; Su JW; Chern SR; Chen YT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
Blancato JK; Eglinton G; George J; Benkendorf J; Pinckert T; Meck J
J Reprod Med; 1995 Jul; 40(7):537-9. PubMed ID: 7473445
[TBL] [Abstract][Full Text] [Related]
11. Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH.
Engelen JJ; Tuerlings JH; Albrechts JC; Schrander-Stumpel CT; Hamers AJ; De Die-Smulders CE
Genet Couns; 2000; 11(1):13-7. PubMed ID: 10756422
[TBL] [Abstract][Full Text] [Related]
12. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
13. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
14. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Santos M; Mrasek K; Rigola MA; Starke H; Liehr T; Fuster C
Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694
[TBL] [Abstract][Full Text] [Related]
15. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Chen CP; Lin HM; Su YN; Chern SR; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2010 Sep; 49(3):341-50. PubMed ID: 21056321
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Chen CP; Chern SR; Lee CC; Chen LF; Chin DT; Tzen CY; Wang W
Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
[TBL] [Abstract][Full Text] [Related]
19. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
Schlegel M; Baumer A; Riegel M; Wiedemann U; Schinzel A
Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
[TBL] [Abstract][Full Text] [Related]
20. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
