268 related articles for article (PubMed ID: 15390181)
21. Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.
Johnston JJ; Walker RL; Davis S; Facio F; Turner JT; Bick DP; Daentl DL; Ellison JW; Meltzer PS; Biesecker LG
J Med Genet; 2007 Jan; 44(1):e59. PubMed ID: 17098889
[TBL] [Abstract][Full Text] [Related]
22. The Greig cephalopolysyndactyly syndrome.
Biesecker LG
Orphanet J Rare Dis; 2008 Apr; 3():10. PubMed ID: 18435847
[TBL] [Abstract][Full Text] [Related]
23. GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease.
Pehlivan T; Pober BR; Brueckner M; Garrett S; Slaugh R; Van Rheeden R; Wilson DB; Watson MS; Hing AV
Am J Med Genet; 1999 Mar; 83(3):201-6. PubMed ID: 10096597
[TBL] [Abstract][Full Text] [Related]
24. Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.
Tanteles GA; Michaelidou S; Loukianou E; Christophidou-Anastasiadou V; Kleopa KA
Clin Dysmorphol; 2015 Jul; 24(3):102-5. PubMed ID: 25714367
[TBL] [Abstract][Full Text] [Related]
25. Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11).
Smith A; Das P; O'Reilly J; Patsouris C; Campbell LJ
Cancer Genet Cytogenet; 2006 Apr; 166(1):86-8. PubMed ID: 16616116
[TBL] [Abstract][Full Text] [Related]
26. Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.
Chotai KA; Brueton LA; van Herwerden L; Garrett C; Hinkel GK; Schinzel A; Mueller RF; Speleman F; Winter RM
Am J Med Genet; 1994 Jul; 51(3):270-6. PubMed ID: 7521123
[TBL] [Abstract][Full Text] [Related]
27. Identification of different Ikaros cDNA transcripts in Philadelphia-positive adult acute lymphoblastic leukemia by a high-throughput capillary electrophoresis sizing method.
Iacobucci I; Lonetti A; Cilloni D; Messa F; Ferrari A; Zuntini R; Ferrari S; Ottaviani E; Arruga F; Paolini S; Papayannidis C; Piccaluga PP; Soverini S; Saglio G; Pane F; Baruzzi A; Vignetti M; Berton G; Vitale A; Chiaretti S; Müschen M; Foà R; Baccarani M; Martinelli G
Haematologica; 2008 Dec; 93(12):1814-21. PubMed ID: 18838475
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Dominant negative isoform of the Ikaros gene in patients with adult B-cell acute lymphoblastic leukemia.
Nakase K; Ishimaru F; Avitahl N; Dansako H; Matsuo K; Fujii K; Sezaki N; Nakayama H; Yano T; Fukuda S; Imajoh K; Takeuchi M; Miyata A; Hara M; Yasukawa M; Takahashi I; Taguchi H; Matsue K; Nakao S; Niho Y; Takenaka K; Shinagawa K; Ikeda K; Niiya K; Harada M
Cancer Res; 2000 Aug; 60(15):4062-5. PubMed ID: 10945610
[TBL] [Abstract][Full Text] [Related]
31. Deletions of interferon genes in acute lymphoblastic leukemia.
Diaz MO; Rubin CM; Harden A; Ziemin S; Larson RA; Le Beau MM; Rowley JD
N Engl J Med; 1990 Jan; 322(2):77-82. PubMed ID: 2294436
[TBL] [Abstract][Full Text] [Related]
32. Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
Johnston JJ; Sapp JC; Turner JT; Amor D; Aftimos S; Aleck KA; Bocian M; Bodurtha JN; Cox GF; Curry CJ; Day R; Donnai D; Field M; Fujiwara I; Gabbett M; Gal M; Graham JM; Hedera P; Hennekam RC; Hersh JH; Hopkin RJ; Kayserili H; Kidd AM; Kimonis V; Lin AE; Lynch SA; Maisenbacher M; Mansour S; McGaughran J; Mehta L; Murphy H; Raygada M; Robin NH; Rope AF; Rosenbaum KN; Schaefer GB; Shealy A; Smith W; Soller M; Sommer A; Stalker HJ; Steiner B; Stephan MJ; Tilstra D; Tomkins S; Trapane P; Tsai AC; Van Allen MI; Vasudevan PC; Zabel B; Zunich J; Black GC; Biesecker LG
Hum Mutat; 2010 Oct; 31(10):1142-54. PubMed ID: 20672375
[TBL] [Abstract][Full Text] [Related]
33. [Greig cephalopolysyndactyly syndrome].
Satokata I
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):184-6. PubMed ID: 11057189
[No Abstract] [Full Text] [Related]
34. The molecular basis of Pallister Hall associated polydactyly.
Hill P; Wang B; Rüther U
Hum Mol Genet; 2007 Sep; 16(17):2089-96. PubMed ID: 17588959
[TBL] [Abstract][Full Text] [Related]
35. The clinical atlas of Greig cephalopolysyndactyly syndrome.
Balk K; Biesecker LG
Am J Med Genet A; 2008 Mar; 146A(5):548-57. PubMed ID: 18241058
[TBL] [Abstract][Full Text] [Related]
36. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
Li T; Xue Y; Zhang J; Chen S; Pan J; Wu Y; Wang Y; Shen J
Cancer Genet Cytogenet; 2008 Feb; 181(1):55-9. PubMed ID: 18262055
[TBL] [Abstract][Full Text] [Related]
37. Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual.
Sobetzko D; Eich G; Kalff-Suske M; Grzeschik KH; Superti-Furga A
Am J Med Genet; 2000 Jan; 90(3):239-42. PubMed ID: 10678662
[TBL] [Abstract][Full Text] [Related]
38. A diminutive chromosome 21 centromere in acute lymphoblastic leukemia.
Roberts KA; Martineau M; Broadfield ZJ; Gibson BE; Harewood L; Stewart J; Harrison CJ
Cancer Genet Cytogenet; 2006 May; 167(1):78-81. PubMed ID: 16682292
[TBL] [Abstract][Full Text] [Related]
39. Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model.
Niida Y; Inoue M; Ozaki M; Takase E
Cytogenet Genome Res; 2017; 153(2):56-65. PubMed ID: 29298444
[TBL] [Abstract][Full Text] [Related]
40. Localization of genes and anonymous DNA probes on the short arm of chromosome 7.
Wagner K; Kroisel PM; Rosenkranz W
Mamm Genome; 1992; 3(1):39-41. PubMed ID: 1316194
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
