72 related articles for article (PubMed ID: 16179228)
1. Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysis.
Matthaei A; Werner W; Gerlach EM; Koerner U; Tinschert S; Nitz I; Herr A; Rump A; Bartsch O; Hinkel KG; Schrock E; Oexle K
Eur J Med Genet; 2005; 48(3):328-38. PubMed ID: 16179228
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
4. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
5. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
6. Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
Kitsiou-Tzeli S; Sismani C; Ioannides M; Bashiardes S; Ketoni A; Touliatou V; Kolialexi A; Mavrou A; Kanavakis E; Patsalis PC
Eur J Med Genet; 2007; 50(1):73-8. PubMed ID: 17194633
[TBL] [Abstract][Full Text] [Related]
7. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
8. Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type.
Menten B; Buysse K; Vandesompele J; De Smet E; De Paepe A; Speleman F; Mortier G
Eur J Med Genet; 2005; 48(3):301-9. PubMed ID: 16179225
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
11. Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
South ST; Whitby H; Battaglia A; Carey JC; Brothman AR
Eur J Hum Genet; 2008 Jan; 16(1):45-52. PubMed ID: 17726485
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
Chaabouni M; Martinovic J; Sanlaville D; Attié-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
[TBL] [Abstract][Full Text] [Related]
13. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
[TBL] [Abstract][Full Text] [Related]
15. Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.
Klopocki E; Neumann LM; Tönnies H; Ropers HH; Mundlos S; Ullmann R
Eur J Hum Genet; 2006 Dec; 14(12):1274-9. PubMed ID: 16896345
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.
Utine EG; Alanay Y; Aktas D; Alikasifoglu M; Boduroglu K; Vermeesch J; Tuncbilek E; Fryns JP
Eur J Med Genet; 2008; 51(4):343-50. PubMed ID: 18440888
[TBL] [Abstract][Full Text] [Related]
18. The human ovarian teratocarcinoma cell line PA-1 demonstrates a single translocation: analysis with fluorescence in situ hybridization, spectral karyotyping, and bacterial artificial chromosome microarray.
Sarraf S; Tejada R; Abawi M; Oberst M; Dennis T; Simon KC; Blancato J
Cancer Genet Cytogenet; 2005 Aug; 161(1):63-9. PubMed ID: 16080959
[TBL] [Abstract][Full Text] [Related]
19. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
20. DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.
Engels H; Brockschmidt A; Hoischen A; Landwehr C; Bosse K; Walldorf C; Toedt G; Radlwimmer B; Propping P; Lichter P; Weber RG
Neurology; 2007 Mar; 68(10):743-50. PubMed ID: 17339581
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
