118 related articles for article (PubMed ID: 26663055)
41. Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).
Saberi A; Shariati G; Hamid M; Galehdari H; Abdorasouli N
Arch Iran Med; 2014 Sep; 17(9):642-4. PubMed ID: 25204484
[TBL] [Abstract][Full Text] [Related]
42. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
He XY; Chen XC; Li R; Li P; Lu AM
Zhongguo Dang Dai Er Ke Za Zhi; 2015 May; 17(5):459-63. PubMed ID: 26014695
[TBL] [Abstract][Full Text] [Related]
43. [Combined spectral karyotyping and microarray-based comparative genomic hybridization for the diagnosis of a case with ring chromosome 15].
Pan M; Choy KW; Liao C; Lau TK
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):562-5. PubMed ID: 23042394
[TBL] [Abstract][Full Text] [Related]
44. CGcgh: a tool for molecular karyotyping using DNA microarray-based comparative genomic hybridization (array-CGH).
Lee YS; Chao A; Chao AS; Chang SD; Chen CH; Wu WM; Wang TH; Wang HS
J Biomed Sci; 2008 Nov; 15(6):687-96. PubMed ID: 18712492
[TBL] [Abstract][Full Text] [Related]
45. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
46. Copy number variations in three children with sudden infant death.
Toruner GA; Kurvathi R; Sugalski R; Shulman L; Twersky S; Pearson PG; Tozzi R; Schwalb MN; Wallerstein R
Clin Genet; 2009 Jul; 76(1):63-8. PubMed ID: 19659761
[TBL] [Abstract][Full Text] [Related]
47. Characteristics of highly polymorphic segmental copy-number variations observed in Japanese by BAC-array-CGH.
Takahashi N; Satoh Y; Sasaki K; Shimoichi Y; Sugita K; Katayama H
J Biomed Biotechnol; 2011; 2011():820472. PubMed ID: 21197411
[TBL] [Abstract][Full Text] [Related]
48. DNA copy number changes and immunophenotype pattern in karyotypically normal acute myeloid leukemia patients from an Indian population.
Kawankar N; Korgaonkar S; Kerketta L; Madkaikar M; Jijina F; Ghosh K; Vundinti BR
Genet Test Mol Biomarkers; 2012 Apr; 16(4):265-70. PubMed ID: 22106833
[TBL] [Abstract][Full Text] [Related]
49. A first comparative map of copy number variations in the sheep genome.
Fontanesi L; Beretti F; Martelli PL; Colombo M; Dall'olio S; Occidente M; Portolano B; Casadio R; Matassino D; Russo V
Genomics; 2011 Mar; 97(3):158-65. PubMed ID: 21111040
[TBL] [Abstract][Full Text] [Related]
50. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
[TBL] [Abstract][Full Text] [Related]
51. Genomic alterations of chromosome region 11p as predictive marker by array comparative genomic hybridization in lung adenocarcinoma patients.
Sung JS; Park KH; Kim YH
Cancer Genet Cytogenet; 2010 Apr; 198(1):27-34. PubMed ID: 20303011
[TBL] [Abstract][Full Text] [Related]
52. Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.
Nordgren A; Corcoran M; Sääf A; Bremer A; Kluin-Nelemans HC; Schoumans J; Grandér D
Eur J Haematol; 2010 Jan; 84(1):17-25. PubMed ID: 19682064
[TBL] [Abstract][Full Text] [Related]
53. Copy number variations identified in the chicken using a 60K SNP BeadChip.
Jia X; Chen S; Zhou H; Li D; Liu W; Yang N
Anim Genet; 2013 Jun; 44(3):276-84. PubMed ID: 23173786
[TBL] [Abstract][Full Text] [Related]
54. Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.
Qiao Y; Liu X; Harvard C; Nolin SL; Brown WT; Koochek M; Holden JJ; Lewis ME; Rajcan-Separovic E
BMC Genomics; 2007 Jun; 8():167. PubMed ID: 17565693
[TBL] [Abstract][Full Text] [Related]
55. [Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].
He WZ; Liu WQ; Zhong XQ; Chen XL; Li SY; Zhang HM; Li Q; Cui QL; Sun XF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):266-9. PubMed ID: 22678785
[TBL] [Abstract][Full Text] [Related]
56. Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.
Napoli E; Russo S; Casula L; Alesi V; Amendola FA; Angioni A; Novelli A; Valeri G; Menghini D; Vicari S
J Autism Dev Disord; 2018 Feb; 48(2):442-449. PubMed ID: 29027068
[TBL] [Abstract][Full Text] [Related]
57. Application of chromosomal microarray in the evaluation of abnormal prenatal findings.
Yatsenko SA; Davis S; Hendrix NW; Surti U; Emery S; Canavan T; Speer P; Hill L; Clemens M; Rajkovic A
Clin Genet; 2013 Jul; 84(1):47-54. PubMed ID: 23020214
[TBL] [Abstract][Full Text] [Related]
58. Benign copy number changes in clinical cytogenetic diagnostics by array CGH.
Whitby H; Tsalenko A; Aston E; Tsang P; Mitchell S; Bayrak-Toydemir P; Hopkins C; Peters G; Bailey DK; Bruhn L; Brothman AR
Cytogenet Genome Res; 2008; 123(1-4):94-101. PubMed ID: 19287143
[TBL] [Abstract][Full Text] [Related]
59. [Reflection of a case misdiagnosed as trisomy 21 syndrome by G-banded chromosomal karyotyping analysis].
Pei X; Liu M; Liu Y; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):1031-1034. PubMed ID: 31598954
[TBL] [Abstract][Full Text] [Related]
60. Copy number variations and stroke.
Colaianni V; Mazzei R; Cavallaro S
Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
