196 related articles for article (PubMed ID: 17937435)
1. Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation.
Borg K; Nowakowska B; Obersztyn E; Cheung SW; Brycz-Witkowska J; Korniszewski L; Mazurczak T; Stankiewicz P; Bocian E
Am J Med Genet A; 2007 Nov; 143A(22):2738-43. PubMed ID: 17937435
[TBL] [Abstract][Full Text] [Related]
2. Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes.
Mendoza-Londono R; Kashork CD; Shaffer LG; Krance R; Plon SE
Genes Chromosomes Cancer; 2005 Jan; 42(1):82-6. PubMed ID: 15390181
[TBL] [Abstract][Full Text] [Related]
3. Greig cephalopolysyndactyly (GCPS) contiguous gene syndrome in a boy with a 14 Mb deletion in region 7p13-14 caused by a paternal balanced insertion (5; 7).
Schulz S; Volleth M; Muschke P; Wieland I; Wieacker P
Appl Clin Genet; 2008; 1():19-22. PubMed ID: 23776344
[TBL] [Abstract][Full Text] [Related]
4. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.
Tyson C; McGillivray B; Chijiwa C; Rajcan-Separovic E
Am J Med Genet A; 2004 Sep; 129A(3):254-60. PubMed ID: 15326624
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
6. Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.
Pettigrew AL; Greenberg F; Caskey CT; Ledbetter DH
Hum Genet; 1991 Aug; 87(4):452-6. PubMed ID: 1879832
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.
Kozma K; Bembea M; Jurca CM; Ioana M; Streață I; Şoşoi SŞ; Pirvu A; Petchesi CD; Szilágyi A; Sava CN; Jurca A; Ujfalusi A; Szűcs Z; Szakszon K
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828280
[TBL] [Abstract][Full Text] [Related]
9. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
[TBL] [Abstract][Full Text] [Related]
10. Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.
Bonnet C; Grégoire MJ; Vibert M; Raffo E; Leheup B; Jonveaux P
J Hum Genet; 2008; 53(10):876-885. PubMed ID: 18651096
[TBL] [Abstract][Full Text] [Related]
11. Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement.
López-Expósito I; Ballesta-Martinez MJ; Bafalliu JA; Vera-Carbonell A; Domingo-Jiménez R; López-González V; Fernández A; Guillén-Navarro E
Genomics; 2014 Apr; 103(4):288-91. PubMed ID: 24607569
[TBL] [Abstract][Full Text] [Related]
12. Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.
Hayashi S; Kurosawa K; Imoto I; Mizutani S; Inazawa J
Am J Med Genet A; 2005 Nov; 139(1):32-6. PubMed ID: 16222686
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
Shetty S; Boycott KM; Gillan TL; Bowser K; Parboosingh JS; McInnes B; Chernos JE; Bernier FP
Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
[TBL] [Abstract][Full Text] [Related]
14. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
[TBL] [Abstract][Full Text] [Related]
15. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
16. A de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactyly.
Karaman B; Rosti RO; Yilmaz K; Oztürk H; Kayserili H; Başaran S
Turk J Pediatr; 2009; 51(6):613-6. PubMed ID: 20196399
[TBL] [Abstract][Full Text] [Related]
17. Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.
Williams PG; Hersh JH; Yen FF; Barch MJ; Kleinert HE; Kunz J; Kalff-Suske M
Clin Genet; 1997 Dec; 52(6):436-41. PubMed ID: 9520255
[TBL] [Abstract][Full Text] [Related]
18. Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.
Vissers LE; Stankiewicz P; Yatsenko SA; Crawford E; Creswick H; Proud VK; de Vries BB; Pfundt R; Marcelis CL; Zackowski J; Bi W; van Kessel AG; Lupski JR; Veltman JA
Hum Genet; 2007 Jul; 121(6):697-709. PubMed ID: 17457615
[TBL] [Abstract][Full Text] [Related]
19. A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation.
Bilguvar K; Bydon M; Bayrakli F; Ercan-Sencicek AG; Bayri Y; Mason C; DiLuna ML; Seashore M; Bronen R; Lifton RP; State M; Gunel M
J Neurosurg; 2007 Dec; 107(6 Suppl):495-9. PubMed ID: 18154020
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.
Borg K; Stankiewicz P; Bocian E; Kruczek A; Obersztyn E; Lupski JR; Mazurczak T
Hum Genet; 2005 Nov; 118(2):267-75. PubMed ID: 16160854
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]