112 related articles for article (PubMed ID: 15047473)
1. [A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances].
Lapierre JM; Sanlaville D; Kang J; Ozilou C; Le Lorc'h M; Waill MC; Prieur M; Colleaux L; Munnich A; Turleau C; Benkhalifa M; Mohammed M; Vekemans M; Romana S
Ann Biol Clin (Paris); 2004; 62(2):203-12. PubMed ID: 15047473
[TBL] [Abstract][Full Text] [Related]
2. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
[TBL] [Abstract][Full Text] [Related]
3. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM
J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449
[TBL] [Abstract][Full Text] [Related]
4. Array comparative genomic hybridization in prenatal diagnosis: another experience.
Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
[TBL] [Abstract][Full Text] [Related]
5. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.
Ness GO; Lybaek H; Houge G
Am J Med Genet; 2002 Nov; 113(2):125-36. PubMed ID: 12407702
[TBL] [Abstract][Full Text] [Related]
6. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM; Prigmore E; Burford DC; Porter KM; Ng BL; Douglas EJ; Fiegler H; Carr P; Kalaitzopoulos D; Clegg S; Sandstrom R; Temple IK; Youings SA; Thomas NS; Dennis NR; Jacobs PA; Crolla JA; Carter NP
J Med Genet; 2005 Jan; 42(1):8-16. PubMed ID: 15635069
[TBL] [Abstract][Full Text] [Related]
7. High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes.
Kirchhoff M; Rose H; Maahr J; Gerdes T; Bugge M; Tommerup N; Tümer Z; Lespinasse J; Jensen PK; Wirth J; Lundsteen C
Eur J Hum Genet; 2000 Sep; 8(9):661-8. PubMed ID: 10980571
[TBL] [Abstract][Full Text] [Related]
8. [Diagnosis of cryptic chromosome aberrations].
Ness GO; Houge G
Tidsskr Nor Laegeforen; 2003 Sep; 123(17):2418-21. PubMed ID: 14562774
[TBL] [Abstract][Full Text] [Related]
9. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation.
Stankiewicz P; Beaudet AL
Curr Opin Genet Dev; 2007 Jun; 17(3):182-92. PubMed ID: 17467974
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
[TBL] [Abstract][Full Text] [Related]
13. [Detection of submicroscopic chromosome abnormalities by comparative genomic hybridization].
Kirchhoff M; Rose H; Gerdes T; Lundsteen C
Ugeskr Laeger; 2001 Oct; 163(41):5652-7. PubMed ID: 11665466
[TBL] [Abstract][Full Text] [Related]
14. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
[TBL] [Abstract][Full Text] [Related]
15. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
[TBL] [Abstract][Full Text] [Related]
16. Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development.
Lybaek H; Meza-Zepeda LA; Kresse SH; Høysaeter T; Steen VM; Houge G
Eur J Hum Genet; 2008 Nov; 16(11):1318-28. PubMed ID: 18461090
[TBL] [Abstract][Full Text] [Related]
17. Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.
Monfort S; Roselló M; Orellana C; Oltra S; Blesa D; Kok K; Ferrer I; Cigudosa JC; Martínez F
J Med Genet; 2008 Jul; 45(7):432-7. PubMed ID: 18413373
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
[TBL] [Abstract][Full Text] [Related]
20. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.
Edelmann L; Hirschhorn K
Ann N Y Acad Sci; 2009 Jan; 1151():157-66. PubMed ID: 19154522
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
