326 related articles for article (PubMed ID: 11491308)
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. Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation.
Tayel SM; Kurczynski TW; Casperson S; McCorquodale MM
Am J Med Genet; 1988 Dec; 31(4):853-61. PubMed ID: 3239578
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
[TBL] [Abstract][Full Text] [Related]
25. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
[TBL] [Abstract][Full Text] [Related]
26. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[TBL] [Abstract][Full Text] [Related]
27. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
[TBL] [Abstract][Full Text] [Related]
28. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
Ayraud N; Galiana A; Llyod M; Deswarte M
Ann Genet; 1976 Mar; 19(1):65-8. PubMed ID: 1084126
[TBL] [Abstract][Full Text] [Related]
29. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
[TBL] [Abstract][Full Text] [Related]
30. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
Blennow E; Bui TH; Wallin A; Kogner P
Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743
[TBL] [Abstract][Full Text] [Related]
31. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
32. DiGeorge anomaly in an infant with deletion of chromosome 22 and dup(9p) due to adjacent type II disjunction.
el-Fouly MH; Higgins JV; Kapur S; Sankey BJ; Matisoff DN; Costa-Fox M
Am J Med Genet; 1991 Mar; 38(4):569-73. PubMed ID: 2063901
[TBL] [Abstract][Full Text] [Related]
33. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
Lee JH; Cho HS; Lee ES; Jung BC
Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
[TBL] [Abstract][Full Text] [Related]
34. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
35. Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p.
Xu J; Freeman V; Carter RF; Paes B; Heshka T; Nowaczyk JM
Am J Med Genet; 2000 Aug; 93(4):285-9. PubMed ID: 10946354
[TBL] [Abstract][Full Text] [Related]
36. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
[TBL] [Abstract][Full Text] [Related]
37. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
Mori MA; Gomar JL; Diaz de Bustamante A; Ananias A; Pinel I; Martinez-Frias ML
Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
[TBL] [Abstract][Full Text] [Related]
38. Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.
Goumy C; Beaufrère AM; Tchirkov A; Gouas L; Gaspard F; Giollant M; Roucaute T; Veronèse L; Lemery D; Vago P
Prenat Diagn; 2008 Feb; 28(2):131-4. PubMed ID: 18236428
[TBL] [Abstract][Full Text] [Related]
39. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
[TBL] [Abstract][Full Text] [Related]
40. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
