146 related articles for article (PubMed ID: 16179225)
1. 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]
2. Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
Chen CP; Lin SP; Tsai FJ; Wang TH; Chern SR; Wang W
Fertil Steril; 2008 Oct; 90(4):1198.e11-8. PubMed ID: 18304539
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
Palka C; Alfonsi M; Morizio E; Soranno A; La Rovere D; Matarrelli B; Rullo AL; Zori R; Chiarelli F; Calabrese G
Eur J Med Genet; 2011; 54(3):333-6. PubMed ID: 21354345
[TBL] [Abstract][Full Text] [Related]
10. Cryptic x; autosome translocation in a boy--delineation of the phenotype.
Jezela-Stanek A; Ciara E; Juszczak M; Pelc M; Materna-Kiryluk A; Krajewska-Walasek M
Pediatr Neurol; 2011 Mar; 44(3):221-4. PubMed ID: 21310340
[TBL] [Abstract][Full Text] [Related]
11. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Chen CP; Lin CC; Li YC; Hsieh LJ; Lee CC; Wang W
Fertil Steril; 2006 Nov; 86(5):1514.e1-2. PubMed ID: 17070202
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.
Kousoulidou L; Parkel S; Zilina O; Palta P; Puusepp H; Remm M; Turner G; Boyle J; van Bokhoven H; de Brouwer A; Van Esch H; Froyen G; Ropers HH; Chelly J; Moraine C; Gecz J; Kurg A; Patsalis PC
Eur J Med Genet; 2007; 50(6):399-410. PubMed ID: 17980689
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
18. Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18.
de Pater JM; Poot M; Beemer FA; Bijlsma JB; Hack WW; Van Dam WM; Eleveld MJ; Loneus WH; Engelen JJ
Eur J Med Genet; 2006; 49(1):19-27. PubMed ID: 16473306
[TBL] [Abstract][Full Text] [Related]
19. Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders.
Wulfsberg EA; Curtis J; Jayne CH
Am J Med Genet; 1992 Jul; 43(5):823-8. PubMed ID: 1642270
[TBL] [Abstract][Full Text] [Related]
20. Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH.
Bukvic N; Carri VD; Di Cosola ML; Pustorino G; Cesarano C; Chetta M; Santacroce R; Sarno M; Sessa F; Longo V; Novelli A; Gentile M; Margaglione M
Am J Med Genet A; 2010 Jul; 152A(7):1730-4. PubMed ID: 20578256
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
