410 related articles for article (PubMed ID: 19372675)
41. Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant.
Lukusa T; Devriendt K; Holvoet M; Fryns JP
Am J Med Genet; 2000 Mar; 91(3):192-7. PubMed ID: 10756341
[TBL] [Abstract][Full Text] [Related]
42. Applications of comparative genomic hybridisation in constitutional chromosome studies.
Breen CJ; Barton L; Carey A; Dunlop A; Glancy M; Hall K; Hegarty AM; Khokhar MT; Power M; Ryan K; Green AJ; Stallings RL
J Med Genet; 1999 Jul; 36(7):511-7. PubMed ID: 10424810
[TBL] [Abstract][Full Text] [Related]
43. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
44. Array painting using microdissected chromosomes to map chromosomal breakpoints.
Backx L; Van Esch H; Melotte C; Kosyakova N; Starke H; Frijns JP; Liehr T; Vermeesch JR
Cytogenet Genome Res; 2007; 116(3):158-66. PubMed ID: 17317954
[TBL] [Abstract][Full Text] [Related]
45. Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14.
Faas BH; Van Der Deure J; Wunderink MI; Merkx G; Brunner HG
Genet Couns; 2006; 17(3):349-57. PubMed ID: 17100204
[TBL] [Abstract][Full Text] [Related]
46. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
[TBL] [Abstract][Full Text] [Related]
47. Direct tandem duplication in chromosome 19q characterized by array CGH.
Palomares Bralo M; Delicado A; Lapunzina P; Velázquez Fragua R; Villa O; Angeles Mori M; Luisa de Torres M; Fernández L; Pérez Jurado LA; López Pajares I
Eur J Med Genet; 2008; 51(3):257-63. PubMed ID: 18342596
[TBL] [Abstract][Full Text] [Related]
48. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
[TBL] [Abstract][Full Text] [Related]
49. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.
Crolla JA
Am J Med Genet; 1998 Feb; 75(4):367-81. PubMed ID: 9482642
[TBL] [Abstract][Full Text] [Related]
50. Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.
Gustavsson P; Schoumans J; Staaf J; Borg A; Nordenskjöld M; Annerén G
Eur J Med Genet; 2007; 50(3):237-41. PubMed ID: 17387046
[TBL] [Abstract][Full Text] [Related]
51. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
Selvarajah S; Yoshimoto M; Ludkovski O; Park PC; Bayani J; Thorner P; Maire G; Squire JA; Zielenska M
Cytogenet Genome Res; 2008; 122(1):5-15. PubMed ID: 18931480
[TBL] [Abstract][Full Text] [Related]
52. Characterization of sSMC by FISH and molecular techniques.
Sheth F; Andrieux J; Ewers E; Kosyakova N; Weise A; Sheth H; Romana SP; LeLorc'h M; Delobel B; Theisen O; Liehr T; Nampoothiri S; Sheth J
Eur J Med Genet; 2011; 54(3):247-55. PubMed ID: 21316495
[TBL] [Abstract][Full Text] [Related]
53. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
Vermeesch JR; Melotte C; Salden I; Riegel M; Trifnov V; Polityko A; Rumyantseva N; Naumchik I; Starke H; Matthijs G; Schinzel A; Fryns JP; Liehr T
Eur J Med Genet; 2005; 48(3):319-27. PubMed ID: 16179227
[TBL] [Abstract][Full Text] [Related]
54. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation.
Bernardini L; Capalbo A; D'Avanzo MG; Torrente I; Grammatico P; Dell'Edera D; Cavalcanti DP; Novelli A; Dallapiccola B
Eur J Med Genet; 2007; 50(2):94-102. PubMed ID: 17236832
[TBL] [Abstract][Full Text] [Related]
55. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
[TBL] [Abstract][Full Text] [Related]
56. Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
Starke H; Mrasek K; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):359-60. PubMed ID: 15750019
[TBL] [Abstract][Full Text] [Related]
57. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].
Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M
Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432
[TBL] [Abstract][Full Text] [Related]
58. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
Li MM; Howard-Peebles PN; Killos LD; Fallon L; Listgarten E; Stanley WS
Prenat Diagn; 2000 Feb; 20(2):138-43. PubMed ID: 10694686
[TBL] [Abstract][Full Text] [Related]
59. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
[TBL] [Abstract][Full Text] [Related]
60. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
