183 related articles for article (PubMed ID: 7516625)
41. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
Chen CP; Lin SP; Chern SR; Tsai FJ; Lee MS; Chen YJ; Wang W
Genet Couns; 2011; 22(4):425-30. PubMed ID: 22303804
[TBL] [Abstract][Full Text] [Related]
42. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
[TBL] [Abstract][Full Text] [Related]
43. De novo trisomy 20p of paternal origin.
Chaabouni M; Turleau C; Karboul L; Jemaa LB; Maazoul F; Attié-Bitach T; Romana S; Chaabouni H
Am J Med Genet A; 2007 May; 143A(10):1100-3. PubMed ID: 17431912
[TBL] [Abstract][Full Text] [Related]
44. [Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features].
Obersztyn E; Klapecki J; Helias-Rodzewicz Z; Bocian E; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):199-209. PubMed ID: 17028389
[TBL] [Abstract][Full Text] [Related]
45. 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]
46. Chromosomal rearrangements detected by FISH and G-banding.
Hou JW; Wang TR
J Formos Med Assoc; 1996 Sep; 95(9):686-91. PubMed ID: 8918057
[TBL] [Abstract][Full Text] [Related]
47. Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.
Friedman JM; Harrod MJ; Howard-Peebles PN
Am J Med Genet; 1992 Sep; 44(1):37-40. PubMed ID: 1519647
[TBL] [Abstract][Full Text] [Related]
48. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
Abuelo D; Mark HF; Bier JA
Clin Pediatr (Phila); 1995 Apr; 34(4):223-6. PubMed ID: 7540523
[No Abstract] [Full Text] [Related]
49. De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes.
Reddy KS; Sulcova V; Young H; Blancato JK; Haddad BR
Am J Med Genet; 1999 Feb; 82(4):318-21. PubMed ID: 10051165
[TBL] [Abstract][Full Text] [Related]
50. Duplication within chromosome 5q characterized by fluorescence in situ hybridization.
Mowat D; Jauch A; Robson L; Smith A
Am J Med Genet; 1999 Apr; 83(5):361-4. PubMed ID: 10232743
[TBL] [Abstract][Full Text] [Related]
51. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
Leclercq S; Maincent K; Baverel F; Tessier DL; Letourneur F; Lebbar A; Dupont JM
Am J Med Genet A; 2009 Mar; 149A(3):437-45. PubMed ID: 19206177
[TBL] [Abstract][Full Text] [Related]
52. Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.
De Brasi D; Rossi E; Giglio S; D'Agostino A; Titomanlio L; Farina V; Andria G; Sebastio G
Am J Med Genet; 2001 Nov; 104(2):127-30. PubMed ID: 11746042
[TBL] [Abstract][Full Text] [Related]
53. Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18.
Wilson GN; Heller KB; Elterman RD; Schneider NR
Am J Med Genet; 1990 Aug; 36(4):506-10. PubMed ID: 1697142
[TBL] [Abstract][Full Text] [Related]
54. Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.
Stankiewicz P; Bocian E; Jakubów-Durska K; Obersztyn E; Lato E; Starke H; Mroczek K; Mazurczak T
J Med Genet; 2000 Feb; 37(2):114-20. PubMed ID: 10662811
[TBL] [Abstract][Full Text] [Related]
55. [Molecular cytogenetic study of a 21p+ variant in a family with Crouzon syndrome].
Fu SM
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1989 Jun; 11(3):165-9. PubMed ID: 2529982
[TBL] [Abstract][Full Text] [Related]
56. Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion.
Yip MY; Kemp J; Hanson N; Wilson M; Purvis-Smith S; Lam-Po-Tang PR
Am J Med Genet; 1989 Jun; 33(2):220-3. PubMed ID: 2764031
[TBL] [Abstract][Full Text] [Related]
57. Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.
van Langen IM; Otter MA; Aronson DC; Overweg-Plandsoen WC; Hennekam RC; Leschot NJ; Hoovers JM
Clin Genet; 1996 Jan; 49(1):49-53. PubMed ID: 8721573
[TBL] [Abstract][Full Text] [Related]
58. Tandem duplication of proximal 5q.
Rojas-Martinez A; Garcia-Cruz D; Medina C; Moller M; Restrepo CM; Rivera H
Ann Genet; 1990; 33(4):228-30. PubMed ID: 1710431
[TBL] [Abstract][Full Text] [Related]
59. Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl.
Barbi G; Spaich C; Adolph S; Kehrer-Sawatzki H
J Med Genet; 2003 Mar; 40(3):e27. PubMed ID: 12624156
[No Abstract] [Full Text] [Related]
60. De novo partial duplication of 17p [dup(17)(p12----p11.2)]: clinical report.
Magenis RE; Brown MG; Allen L; Reiss J
Am J Med Genet; 1986 Jul; 24(3):415-20. PubMed ID: 2425620
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
