974 related articles for article (PubMed ID: 16506269)
21. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
[TBL] [Abstract][Full Text] [Related]
24. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
Scott JA; Wenger SL; Steele MW; Chakravarti A
Am J Med Genet; 1995 Mar; 56(1):67-71. PubMed ID: 7747789
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
Chen CP; Liou JD; Seow KM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
[TBL] [Abstract][Full Text] [Related]
26. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
30. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
[TBL] [Abstract][Full Text] [Related]
31. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
[TBL] [Abstract][Full Text] [Related]
33. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
[TBL] [Abstract][Full Text] [Related]
34. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.
Chen CP; Lin YH; Chou SY; Su YN; Chern SR; Chen YT; Town DD; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):71-6. PubMed ID: 22482972
[TBL] [Abstract][Full Text] [Related]
35. Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.
Cardoso LC; Moraes L; Camilo MJ; Mulatinho MV; Ramos H; Almeida JC; Llerena JC; Seuánez HN; Vargas FR
Eur J Med Genet; 2008; 51(6):588-97. PubMed ID: 18674646
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Prenatal diagnosis of complete trisomy 19q.
Babić I; Brajenović-Milić B; Petrović O; Mustać E; Kapović M
Prenat Diagn; 2007 Jul; 27(7):644-7. PubMed ID: 17437325
[TBL] [Abstract][Full Text] [Related]
39. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
Riegel M; Baumer A; Piram A; Ortolan D; Peres LC; Pina-Neto JM
Genet Couns; 2001; 12(1):69-75. PubMed ID: 11332980
[TBL] [Abstract][Full Text] [Related]
40. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
