194 related articles for article (PubMed ID: 16240409)
1. The use of genomic microarrays to study chromosomal abnormalities in mental retardation.
Mao R; Pevsner J
Ment Retard Dev Disabil Res Rev; 2005; 11(4):279-85. PubMed ID: 16240409
[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. 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]
4. X chromosome array-CGH for the identification of novel X-linked mental retardation genes.
Bauters M; Van Esch H; Marynen P; Froyen G
Eur J Med Genet; 2005; 48(3):263-75. PubMed ID: 16179222
[TBL] [Abstract][Full Text] [Related]
5. Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.
Vissers LE; de Vries BB; Veltman JA
J Med Genet; 2010 May; 47(5):289-97. PubMed ID: 19951919
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.
Malan V; Raoul O; Firth HV; Royer G; Turleau C; Bernheim A; Willatt L; Munnich A; Vekemans M; Lyonnet S; Cormier-Daire V; Colleaux L
J Med Genet; 2009 Sep; 46(9):635-40. PubMed ID: 19126570
[TBL] [Abstract][Full Text] [Related]
11. A 400kb duplication, 2.4Mb triplication and 130kb duplication of 9q34.3 in a patient with severe mental retardation.
Gijsbers AC; Bijlsma EK; Weiss MM; Bakker E; Breuning MH; Hoffer MJ; Ruivenkamp CA
Eur J Med Genet; 2008; 51(5):479-87. PubMed ID: 18547887
[TBL] [Abstract][Full Text] [Related]
12. Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
Froyen G; Van Esch H; Bauters M; Hollanders K; Frints SG; Vermeesch JR; Devriendt K; Fryns JP; Marynen P
Hum Mutat; 2007 Oct; 28(10):1034-42. PubMed ID: 17546640
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Screening for submicroscopic chromosomal rearrangements in Wilms tumor using whole-genome microarrays.
Rassekh SR; Chan S; Harvard C; Dix D; Qiao Y; Rajcan-Separovic E
Cancer Genet Cytogenet; 2008 Apr; 182(2):84-94. PubMed ID: 18406869
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
Reutter H; Hoischen A; Ludwig M; Stein R; Radlwimmer B; Engels H; Wolffenbuttel KP; Weber RG
BJU Int; 2007 Sep; 100(3):646-50. PubMed ID: 17669146
[TBL] [Abstract][Full Text] [Related]
18. Genomic microarrays in clinical diagnosis.
Veltman JA
Curr Opin Pediatr; 2006 Dec; 18(6):598-603. PubMed ID: 17099357
[TBL] [Abstract][Full Text] [Related]
19. Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
Jaillard S; Drunat S; Bendavid C; Aboura A; Etcheverry A; Journel H; Delahaye A; Pasquier L; Bonneau D; Toutain A; Burglen L; Guichet A; Pipiras E; Gilbert-Dussardier B; Benzacken B; Martin-Coignard D; Henry C; David A; Lucas J; Mosser J; David V; Odent S; Verloes A; Dubourg C
Eur J Med Genet; 2010; 53(2):66-75. PubMed ID: 19878743
[TBL] [Abstract][Full Text] [Related]
20. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]