143 related articles for article (PubMed ID: 11536263)
21. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
22. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
[TBL] [Abstract][Full Text] [Related]
24. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of trisomy 6 mosaicism.
Destree A; Fourneau C; Dugauquier C; Rombout S; Sartenaer D; Gillerot Y
Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis of trisomy 1q21-qter: case report and review of literature.
Machlitt A; Kuepferling P; Bommer C; Koerner H; Chaoui R
Am J Med Genet A; 2005 Apr; 134A(2):207-11. PubMed ID: 15704122
[TBL] [Abstract][Full Text] [Related]
27. Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings.
Cakmak-Genc G; Karakas-Celik S; Dursun A; Piskin İE
Gene; 2015 Sep; 568(2):211-4. PubMed ID: 25979671
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
[TBL] [Abstract][Full Text] [Related]
30. A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9).
Hengstschläger M; Bettelheim D; Repa C; Lang S; Deutinger J; Bernaschek G
Fetal Diagn Ther; 2002; 17(4):243-6. PubMed ID: 12065954
[TBL] [Abstract][Full Text] [Related]
31. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
[TBL] [Abstract][Full Text] [Related]
32. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
33. Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations.
Speleman F; Callens B; Logghe K; Van Roy N; Horsley SW; Jauch A; Verschraegen-Spae MR; Leroy JG
Am J Med Genet; 2000 Aug; 93(5):349-54. PubMed ID: 10951456
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of der(11)t(11;18)(q24;q21.3) due to paternal balanced translocation and both parents are carriers of alpha-thalassemia-1--a case report.
Chao MC; Yang SY; Chang Y; Huang YW; Liu TC; Lee JP; Chen BH
Kaohsiung J Med Sci; 2001 Aug; 17(8):430-6. PubMed ID: 11715843
[TBL] [Abstract][Full Text] [Related]
35. Duplication/deletion mosaicism of the 7q(21.1 --> 31.3) region.
Morales C; Madrigal I; Esqué T; de la Fuente JE; Rodríguez JM; Margarit E; Soler A; Sánchez A
Am J Med Genet A; 2007 Jan; 143A(2):179-83. PubMed ID: 17163539
[TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.
Chen CP; Wang TH; Lin CC; Tsai FJ; Hsieh LJ; Wang W
J Formos Med Assoc; 2008 Oct; 107(10):822-6. PubMed ID: 18926951
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.
Atik T; Durmaz B; Yorganci OU; Cogulu O; Kioutsouk M; Ozkinay F
Genet Couns; 2013; 24(2):179-84. PubMed ID: 24032288
[TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
[TBL] [Abstract][Full Text] [Related]
40. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]