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Items: 1 to 20 of 92

1.

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.

Sagoo GS, Butterworth AS, Sanderson S, Shaw-Smith C, Higgins JP, Burton H.

Genet Med. 2009 Mar;11(3):139-46. doi: 10.1097/GIM.0b013e318194ee8f. Review.

PMID:
19367186
2.

Array-based comparative genomic hybridization for investigating chromosomal abnormalities in patients with learning disability: systematic review meta-analysis of diagnostic and false-positive yields.

Subramonia-Iyer S, Sanderson S, Sagoo G, Higgins J, Burton H, Zimmern R, Kroese M, Brice P, Shaw-Smith C.

Genet Med. 2007 Feb;9(2):74-9.

PMID:
17304048
3.

[Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].

Vorsanova SG, Iurov IIu, Kurinnaia OS, Voinova VIu, Iurov IuB.

Zh Nevrol Psikhiatr Im S S Korsakova. 2013;113(8):46-9. Russian.

PMID:
24077551
4.

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.

de Leeuw N, Hehir-Kwa JY, Simons A, Geurts van Kessel A, Smeets DF, Faas BH, Pfundt R.

Cytogenet Genome Res. 2011;135(3-4):212-21. doi: 10.1159/000331273. Epub 2011 Sep 16. Review.

PMID:
21934286
5.

[Array comparative genomic hybridization detection of a de novo 4q21.21-q22.1 deletion in a child with severe growth retardation].

Zhou J, Hu P, Liu A, Li L, Ji X, Hui W, Wang Y, Xu Z.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):52-5. doi: 10.3760/cma.j.issn.1003-9406.2014.01.012. Chinese.

PMID:
24510563
6.

The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.

Bartnik M, Wiśniowiecka-Kowalnik B, Nowakowska B, Smyk M, Kędzior M, Sobecka K, Kutkowska-Kaźmierczak A, Klapecki J, Szczałuba K, Castañeda J, Własienko P, Bezniakow N, Obersztyn E, Bocian E.

Dev Period Med. 2014 Jul-Sep;18(3):307-17.

7.

Array CGH analysis of a cohort of Russian patients with intellectual disability.

Kashevarova AA, Nazarenko LP, Skryabin NA, Salyukova OA, Chechetkina NN, Tolmacheva EN, Sazhenova EA, Magini P, Graziano C, Romeo G, Kučinskas V, Lebedev IN.

Gene. 2014 Feb 15;536(1):145-50. doi: 10.1016/j.gene.2013.11.029. Epub 2013 Nov 27.

PMID:
24291026
8.

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.

Tzetis M, Kitsiou-Tzeli S, Frysira H, Xaidara A, Kanavakis E.

Expert Rev Mol Diagn. 2012 Jun;12(5):449-57. doi: 10.1586/erm.12.40.

PMID:
22702362
9.

Cytogenomic Evaluation of Children with Congenital Anomalies: Critical Implications for Diagnostic Testing and Genetic Counseling.

Szczałuba K, Jakubiuk-Tomaszuk A, Kędzior M, Bernaciak J, Zdrodowska J, Kurzątkowski W, Radkowski M, Demkow U.

Adv Exp Med Biol. 2016;912:11-9. doi: 10.1007/5584_2016_234.

PMID:
26987321
10.
11.

Use of array-based technology in the practice of medical genetics.

Manning M, Hudgins L.

Genet Med. 2007 Sep;9(9):650-3.

PMID:
17873654
12.

Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances.

Emy Dorfman L, Leite JC, Giugliani R, Riegel M.

J Pediatr (Rio J). 2015 Jan-Feb;91(1):59-67. doi: 10.1016/j.jped.2014.05.007. Epub 2014 Sep 6.

13.

[Diagnosis of chromosomal abnormalities by array CGH in constitutional pathology: the end of the first-line karyotype].

Malan V, Romana S.

Arch Pediatr. 2012 Apr;19(4):437-42. doi: 10.1016/j.arcped.2012.01.004. Epub 2012 Feb 17. Review. French.

PMID:
22342099
14.

Analysis of chromosomal aberrations in patients with mental retardation using the array-CGH technique: a single Czech centre experience.

Zrnová E, Vranová V, Slámová I, Gaillyová R, Kuglík P.

Folia Biol (Praha). 2011;57(5):206-15.

15.

Array-CGH in children with mild intellectual disability: a population-based study.

Coutton C, Dieterich K, Satre V, Vieville G, Amblard F, David M, Cans C, Jouk PS, Devillard F.

Eur J Pediatr. 2015 Jan;174(1):75-83. doi: 10.1007/s00431-014-2367-6. Epub 2014 Jul 3.

PMID:
24985125
16.

Chromosomal microarray (CMA) analysis in infants with congenital anomalies: when is it really helpful?

Resta N, Memo L.

J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 4:124-6. doi: 10.3109/14767058.2012.715004. Review.

PMID:
22958042
17.

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
18.

[Array CGH: technical considerations and applications].

Sireteanu A, Covic M, Gorduza EV.

Rev Med Chir Soc Med Nat Iasi. 2012 Apr-Jun;116(2):545-51. Review. Romanian.

PMID:
23077951
19.

Application of array-based comparative genome hybridization in children with developmental delay or mental retardation.

Liang JS, Shimojima K, Yamamoto T.

Pediatr Neonatol. 2008 Dec;49(6):213-7. doi: 10.1016/S1875-9572(09)60013-9. Review. Erratum in: Pediatr Neonatol. 2009 Feb;50(1):39.

20.

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Shoukier M, Klein N, Auber B, Wickert J, Schröder J, Zoll B, Burfeind P, Bartels I, Alsat EA, Lingen M, Grzmil P, Schulze S, Keyser J, Weise D, Borchers M, Hobbiebrunken E, Röbl M, Gärtner J, Brockmann K, Zirn B.

Clin Genet. 2013 Jan;83(1):53-65. doi: 10.1111/j.1399-0004.2012.01850.x. Epub 2012 Feb 21.

PMID:
22283495

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