136 related articles for article (PubMed ID: 20155755)
1. A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
Valduga M; Philippe C; Bach Segura P; Thiebaugeorges O; Miton A; Beri M; Bonnet C; Nemos C; Foliguet B; Jonveaux P
Prenat Diagn; 2010 Apr; 30(4):333-41. PubMed ID: 20155755
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
[TBL] [Abstract][Full Text] [Related]
7. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
D'Amours G; Kibar Z; Mathonnet G; Fetni R; Tihy F; Désilets V; Nizard S; Michaud JL; Lemyre E
Clin Genet; 2012 Feb; 81(2):128-41. PubMed ID: 21496010
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
Machado IN; Heinrich JK; Barini R; Peralta CF
Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion 6p22.3-p24.3 characterized by CGH array in a foetus with multiple malformations.
Colmant C; Brisset S; Tachdjian G; Gautier V; Ftouki M; Laroudie M; Druart L; Frydman R; Picone O
Prenat Diagn; 2009 Sep; 29(9):908-10. PubMed ID: 19530104
[No Abstract] [Full Text] [Related]
12. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
13. Efficacy of array comparative genomic hybridization in a fetus with an inherited apparently balanced translocation: A case report.
Park JK; Lee JI; Jo HC; Shin JK; Lee SA; Lee JH; Paik WY
J Obstet Gynaecol Res; 2008 Aug; 34(4 Pt 2):653-7. PubMed ID: 18840174
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
[TBL] [Abstract][Full Text] [Related]
18. Clinical utility of array comparative genomic hybridisation in prenatal setting.
Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B
BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804
[TBL] [Abstract][Full Text] [Related]
19. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
[TBL] [Abstract][Full Text] [Related]
20. The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformations.
Goemaere N; Douben H; Van Opstal D; Wouters C; Tibboel D; de Krijger R; de Klein A
Pediatr Dev Pathol; 2010; 13(2):85-94. PubMed ID: 19594201
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]