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Results: 1 to 20 of 117

Related Citations for PubMed (Select 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. doi: 10.1002/pd.2460.

PMID:
20155755
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.

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. doi: 10.1159/000224112. Epub 2009 Jun 11.

PMID:
19521095
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. doi: 10.1111/j.1471-0528.2012.03279.x. Epub 2012 Feb 7.

PMID:
22313859
5.
6.

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.

Kleeman L, Bianchi DW, Shaffer LG, Rorem E, Cowan J, Craigo SD, Tighiouart H, Wilkins-Haug LE.

Prenat Diagn. 2009 Dec;29(13):1213-7. doi: 10.1002/pd.2367.

PMID:
19862770
7.

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 Sep-Oct;52(5):291-6. doi: 10.1016/j.ejmg.2009.05.011. Epub 2009 Jun 6.

PMID:
19505601
8.

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.

PMID:
20420025
9.

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. doi: 10.1111/j.1399-0004.2011.01687.x. Epub 2011 May 16.

PMID:
21496010
10.

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL.

Clin Chem. 2007 Dec;53(12):2051-9. Epub 2007 Sep 27.

11.

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. doi: 10.1111/j.1749-6632.2008.03610.x. Review.

PMID:
19154522
12.

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 15;10(1):261-7. doi: 10.4238/vol10-1gmr1001.

13.

Application of metaphase HR-CGH and targeted Chromosomal Microarray Analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features.

Nowakowska B, Stankiewicz P, Obersztyn E, Ou Z, Li J, Chinault AC, Smyk M, Borg K, Mazurczak T, Cheung SW, Bocian E.

Am J Med Genet A. 2008 Sep 15;146A(18):2361-9. doi: 10.1002/ajmg.a.32475.

PMID:
18698622
14.

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 16;9(1):441-8. doi: 10.4238/vol9-1gmr716.

15.

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. doi: 10.1002/pd.2306. No abstract available.

PMID:
19530104
16.

Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.

Cain CC, Saul DO, Oehler E, Blakemore K, Stetten G.

Fetal Diagn Ther. 2008;24(3):286-90. doi: 10.1159/000158519. Epub 2008 Sep 26.

PMID:
18818501
17.

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.

PMID:
16450348
18.

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

Hannes FD, Sharp AJ, Mefford HC, de Ravel T, Ruivenkamp CA, Breuning MH, Fryns JP, Devriendt K, Van Buggenhout G, Vogels A, Stewart H, Hennekam RC, Cooper GM, Regan R, Knight SJ, Eichler EE, Vermeesch JR.

J Med Genet. 2009 Apr;46(4):223-32. doi: 10.1136/jmg.2007.055202. Epub 2008 Jun 11.

19.

Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.

Alvarado M, Bass HN, Caldwell S, Jamehdor M, Miller AA, Jacob P.

Am J Dis Child. 1993 Dec;147(12):1291-4.

PMID:
8249946
20.

Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH).

Hung CC, Lin CH, Lin SY, Shin JC, Lee CN, Su YN.

Gene. 2012 Mar 10;495(2):178-82. doi: 10.1016/j.gene.2011.12.050. Epub 2012 Jan 3.

PMID:
22248625
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