453 related articles for article (PubMed ID: 24677787)
21. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay.
Bose D; Krishnamurthy V; Venkatesh KS; Aiyaz M; Shetty M; Rao SN; Kutty AV
Cytogenet Genome Res; 2015; 145(1):14-8. PubMed ID: 25896599
[TBL] [Abstract][Full Text] [Related]
22. Partial trisomy 11q and partial monosomy 12p due to the maternal translocation (11q;12p).
Tos T; Alp MY; Eker HK; Cebi AH; Okumus N; Ikbal M
Genet Couns; 2013; 24(3):343-5. PubMed ID: 24341151
[No Abstract] [Full Text] [Related]
23. Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21).
Yelavarthi KK; Zunich J
Am J Med Genet A; 2004 May; 126A(4):423-6. PubMed ID: 15098242
[TBL] [Abstract][Full Text] [Related]
24. Mild phenotype in two siblings with distal monosomy 12p13.31-->pter.
Glass IA; Trenholme A; Mildenhall L; Bailey RJ; Cotter PD
Clin Genet; 2000 May; 57(5):401-5. PubMed ID: 10852377
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature.
Ben-Abdallah-Bouhjar I; Mougou-Zerelli S; Hannachi H; Ben-Khelifa H; Soyah N; Labalme A; Sanlaville D; Elghezal H; Saad A
Gene; 2013 Apr; 519(1):135-41. PubMed ID: 23403231
[TBL] [Abstract][Full Text] [Related]
27. Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report.
Say B; Guzoglu N; Uras N; Candemir Z; Akin I; Dilmen U
Genet Couns; 2013; 24(4):387-91. PubMed ID: 24551981
[TBL] [Abstract][Full Text] [Related]
28. De-novo 'pure' partial trisomy (6)(p22.3→pter): a case report and review of the literature.
Sivasankaran A; Murthy K; Oruganti VP; Deenadayalu A; R Samuel C; Kandukuri LR
Clin Dysmorphol; 2017 Jan; 26(1):26-32. PubMed ID: 27759572
[TBL] [Abstract][Full Text] [Related]
29. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
Zumkeller W; Volleth M; Muschke P; Tönnies H; Heller A; Liehr T; Wieacker P; Stumm M
Am J Med Genet A; 2004 Sep; 129A(3):261-4. PubMed ID: 15326625
[TBL] [Abstract][Full Text] [Related]
30. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
[TBL] [Abstract][Full Text] [Related]
31. Partial trisomy 17q and partial monosomy 20q in a boy with craniosynostosis.
Marques F; Heredia R; de Oliveira C; Cardoso MT; Mazzeu J; Pogue R
Am J Med Genet A; 2015 Feb; 167A(2):412-6. PubMed ID: 25424318
[TBL] [Abstract][Full Text] [Related]
32. 17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature.
Rasmussen M; Vestergaard EM; Graakjaer J; Petkov Y; Bache I; Fagerberg C; Kibaek M; Svaneby D; Petersen OB; Brasch-Andersen C; Sunde L
Am J Med Genet A; 2016 Nov; 170(11):2934-2942. PubMed ID: 27409573
[TBL] [Abstract][Full Text] [Related]
33. Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings.
Kayhan G; Cavdarli B; Yirmibes Karaoguz M; Percin EF; Oztürk Kaymak A; Biri A; Ergun MA
Gene; 2013 Jul; 524(2):355-60. PubMed ID: 23644025
[TBL] [Abstract][Full Text] [Related]
34. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation.
Hosono K; Kawase K; Kurata K; Niimi Y; Saitsu H; Minoshima S; Ohnishi H; Yamamoto T; Hikoya A; Tachibana N; Fukao T; Yamamoto T; Hotta Y
Ophthalmic Genet; 2020 Apr; 41(2):175-182. PubMed ID: 32223580
[No Abstract] [Full Text] [Related]
35. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
[TBL] [Abstract][Full Text] [Related]
36. Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.
Van Der Burgt CJ; Merkx GF; Janssen AH; Mulder JC; Suijkerbuijk RF; Smeets DF
J Med Genet; 1992 Oct; 29(10):739-41. PubMed ID: 1433237
[TBL] [Abstract][Full Text] [Related]
37. Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies.
Walker A; Wang X; Kim YM; Lu X; Taylor A; Demarzo D; Li S; Pang H
Mol Cytogenet; 2022 Apr; 15(1):17. PubMed ID: 35440058
[TBL] [Abstract][Full Text] [Related]
38. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: molecular characterization of two der(11)t(11;16).
Basinko A; Audebert-Bellanger S; Douet-Guilbert N; Le Franc J; Parent P; Quemener S; La Selve P; Bovo C; Morel F; Le Bris MJ; De Braekeleer M
Am J Med Genet A; 2011 Sep; 155A(9):2281-7. PubMed ID: 21834034
[TBL] [Abstract][Full Text] [Related]
39. Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.
Schmidt B; Udink ten Cate F; Weiss M; Koehler U
Eur J Pediatr; 2012 Jul; 171(7):1047-53. PubMed ID: 22302461
[TBL] [Abstract][Full Text] [Related]
40. Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies.
Luo M; Mulchandani S; Dubbs HA; Swarr D; Pyle L; Zackai EH; Spinner NB; Conlin LK
Am J Med Genet A; 2015 Dec; 167A(12):3091-5. PubMed ID: 26198585
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
