789 related articles for article (PubMed ID: 17515297)
21. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
[TBL] [Abstract][Full Text] [Related]
22. Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18.
de Pater JM; Poot M; Beemer FA; Bijlsma JB; Hack WW; Van Dam WM; Eleveld MJ; Loneus WH; Engelen JJ
Eur J Med Genet; 2006; 49(1):19-27. PubMed ID: 16473306
[TBL] [Abstract][Full Text] [Related]
23. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
[TBL] [Abstract][Full Text] [Related]
24. Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.
Utine GE; Aktas D; Boduroğlu K; Alikasifoğlu M; Tunçbilek E
Genet Couns; 2007; 18(2):171-7. PubMed ID: 17710869
[TBL] [Abstract][Full Text] [Related]
25. Partial 3q trisomy due to an unbalanced 3/10 translocation.
Blumberg B; Moore R; Mohandas T
Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
[TBL] [Abstract][Full Text] [Related]
26. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
27. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
28. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.
Sun SC; Luo FW; Song HW; He JB; Peng YS
J Int Med Res; 2009; 37(4):1230-7. PubMed ID: 19761709
[TBL] [Abstract][Full Text] [Related]
29. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
Chen CP; Lin SP; Lee CC; Town DD; Wang W
Genet Couns; 2006; 17(3):301-6. PubMed ID: 17100198
[TBL] [Abstract][Full Text] [Related]
30. [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]
31. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
[TBL] [Abstract][Full Text] [Related]
32. Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
Hou JW
J Formos Med Assoc; 2003 Dec; 102(12):887-92. PubMed ID: 14976570
[TBL] [Abstract][Full Text] [Related]
33. Trisomy 22: no longer an enigma.
Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
[TBL] [Abstract][Full Text] [Related]
34. Unbalanced 4;6 translocation and progressive renal disease.
Pierpont ME; Hentges AS; Gears LJ; Hirsch B; Sinaiko A
Am J Med Genet; 2000 Nov; 95(3):275-80. PubMed ID: 11102935
[TBL] [Abstract][Full Text] [Related]
35. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.
Yamada K; Uchiyama A; Arai M; Kubodera K; Yamamoto Y; Orii KO; Nagasawa H; Masuno M; Kohno Y
Congenit Anom (Kyoto); 2009 Jun; 49(2):85-8. PubMed ID: 19489960
[TBL] [Abstract][Full Text] [Related]
38. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
Zafra de la Rosa G; Venegas-Vega CA; Monroy N; Contreras-Bucio G; Friedrich U; Houman M; Saad A; Fernández P; Kofman-Alfaro S; Cervantes A
Am J Med Genet A; 2005 Jul; 136(3):259-64. PubMed ID: 15957183
[TBL] [Abstract][Full Text] [Related]
39. Partial monosomy 11q and trisomy 12q: variable expression in two siblings.
Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP
Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809
[TBL] [Abstract][Full Text] [Related]
40. Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
Wieczorek D; Bartsch O; Gillessen-Kaesbach G
Am J Med Genet A; 2003 Jul; 120A(3):429-33. PubMed ID: 12838568
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
