226 related articles for article (PubMed ID: 22925348)
21. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
24. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
[TBL] [Abstract][Full Text] [Related]
25. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Chern SR; Chen WM; Lee CC; Hsieh LJ; Wang W
Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
[TBL] [Abstract][Full Text] [Related]
26. Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes.
Byatt SA; Baker E; Richards RI; Roberts C; Smith A
Am J Med Genet; 1997 Jun; 70(4):357-60. PubMed ID: 9182774
[TBL] [Abstract][Full Text] [Related]
27. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
31. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
32. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
Chen CP; Lin SP; Su YN; Tsai FJ; Wu PC; Town DD; Chen LF; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation.
Petek E; Wagner K; Steiner H; Schaffer H; Kroisel PM
Prenat Diagn; 2000 Apr; 20(4):349-52. PubMed ID: 10740212
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.
Sung PL; Chang CM; Chen CY; Wang PH; Chao KC; Wen KC; Cheng YY; Li YC; Lin CC
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):260-5. PubMed ID: 22795105
[TBL] [Abstract][Full Text] [Related]
35. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
36. 1q44-qter trisomy: clinical report and review of the literature.
Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
Chen CP; Lin CC; Chang TY; Li YC; Hsieh LJ; Lee CC; Chen LF; Wang W
Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
[No Abstract] [Full Text] [Related]
38. 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]
39. Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7).
Courtens W; Vroman S; Vandenhove J; Wiedemann U; Schinzel A
Prenat Diagn; 2001 Aug; 21(8):642-8. PubMed ID: 11536263
[TBL] [Abstract][Full Text] [Related]
40. Prenatal overgrowth and mosaic trisomy 15q25-qter including the IGF1 receptor gene.
Faivre L; Rousseau T; Laurent N; Gosset P; Sanlaville D; Thauvin-Robinet C; Cusin V; Lionnais S; Callier P; Khau Van Kien P; Huet F; Turleau C; Sagot P; Mugneret F
Prenat Diagn; 2004 May; 24(5):393-5. PubMed ID: 15164417
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]