168 related articles for article (PubMed ID: 16082706)
21. Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.
Pedurupillay CR; Misceo D; Gamage TH; Dissanayake VH; Frengen E
Gene; 2014 Jan; 533(1):403-10. PubMed ID: 24095780
[TBL] [Abstract][Full Text] [Related]
22. Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23).
Drazinic CM; Ercan-Sencicek AG; Gault LM; Hisama FM; Qumsiyeh MB; Nowak NJ; Cubells JF; State MW
Am J Med Genet A; 2005 Apr; 134(3):282-9. PubMed ID: 15754353
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
[TBL] [Abstract][Full Text] [Related]
25. Mosaic isodicentric chromosome 18q: sixth report and review.
Oudesluijs GG; Hulzebos CV; Sikkema-Raddatz B; Van Essen AJ
Genet Couns; 2006; 17(4):395-400. PubMed ID: 17375524
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.
Yatsenko SA; Treadwell-Deering D; Krull K; Lewis RA; Glaze D; Stankiewicz P; Lupski JR; Potocki L
Am J Med Genet A; 2005 Oct; 138A(2):175-80. PubMed ID: 16152635
[TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
29. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
Liang D; Wu L; Pan Q; Harada N; Long Z; Xia K; Yoshiura K; Dai H; Niikawa N; Cai F; Xia J
Am J Med Genet A; 2006 Feb; 140(3):238-44. PubMed ID: 16411213
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
[TBL] [Abstract][Full Text] [Related]
31. Prenatal detection of monosomy 18p and trisomy 18q mosaicism with unexpected fetal phenotype.
Sutton SD; Ridler MA
J Med Genet; 1986 Jun; 23(3):258-9. PubMed ID: 3723556
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of mosaic tetrasomy 18p.
Chen CP; Ko TM; Su YN; Chern SR; Su JW; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Dec; 51(4):625-9. PubMed ID: 23276569
[TBL] [Abstract][Full Text] [Related]
33. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
[TBL] [Abstract][Full Text] [Related]
34. [A case of pseudoisodicentric chromosome 18q detected at prenatal diagnosis].
Cho SY; Lim G; Kim SY; Kim MJ; Lee KA; Choi JR; Lee HJ; Suh JT; Park TS; Jung E
Korean J Lab Med; 2010 Aug; 30(4):440-3. PubMed ID: 20805718
[TBL] [Abstract][Full Text] [Related]
35. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.
Boghosian-Sell L; Mewar R; Harrison W; Shapiro RM; Zackai EH; Carey J; Davis-Keppen L; Hudgins L; Overhauser J
Am J Hum Genet; 1994 Sep; 55(3):476-83. PubMed ID: 8079991
[TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.
Hu H; Hao J; Yao H; Chang Q; Li R; Zhang X; Liang Z
Gene; 2013 Mar; 517(1):132-6. PubMed ID: 23232358
[TBL] [Abstract][Full Text] [Related]
37. Different conformation of two supernumerary 18p isochromosomes, one with a concomitant partial 18q trisomy.
Noronha Dutra AR; Mancini TI; Satomi Takeno S; Moysés Oliveira M; Kim CA; Alvarez Perez AB; Domenici Kulikowski L; Melaragno MI
Cytogenet Genome Res; 2012; 138(1):1-4. PubMed ID: 22796746
[TBL] [Abstract][Full Text] [Related]
38. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.
Fan YS; Siu VM
Am J Med Genet; 2001 Aug; 102(3):266-71. PubMed ID: 11484205
[TBL] [Abstract][Full Text] [Related]
39. Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.
Gereltzul E; Baba Y; Suda N; Shiga M; Inoue MS; Tsuji M; Shin I; Hirata Y; Ohyama K; Moriyama K
J Hum Genet; 2008; 53(10):941-946. PubMed ID: 18679767
[TBL] [Abstract][Full Text] [Related]
40. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
