270 related articles for article (PubMed ID: 15390181)
1. 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]
2. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
Vortkamp A; Gessler M; Grzeschik KH
Nature; 1991 Aug; 352(6335):539-40. PubMed ID: 1650914
[TBL] [Abstract][Full Text] [Related]
3. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
Kang S; Graham JM; Olney AH; Biesecker LG
Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region.
Vortkamp A; Gessler M; Le Paslier D; Elaswarapu R; Smith S; Grzeschik KH
Genomics; 1994 Aug; 22(3):563-8. PubMed ID: 8001967
[TBL] [Abstract][Full Text] [Related]
6. Birth defects caused by mutations in human GLI3 and mouse Gli3 genes.
Naruse I; Ueta E; Sumino Y; Ogawa M; Ishikiriyama S
Congenit Anom (Kyoto); 2010 Mar; 50(1):1-7. PubMed ID: 20201963
[TBL] [Abstract][Full Text] [Related]
7. Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS).
Schwarzbraun T; Windpassinger C; Ofner L; Vincent JB; Cheung J; Scherer SW; Wagner K; Kroisel PM; Petek E
Eur J Med Genet; 2006; 49(4):338-45. PubMed ID: 16829355
[TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I.
Fujioka H; Ariga T; Horiuchi K; Otsu M; Igawa H; Kawashima K; Yamamoto Y; Sugihara T; Sakiyama Y
Clin Genet; 2005 May; 67(5):429-33. PubMed ID: 15811011
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.
Johnston JJ; Olivos-Glander I; Turner J; Aleck K; Bird LM; Mehta L; Schimke RN; Heilstedt H; Spence JE; Blancato J; Biesecker LG
Am J Med Genet A; 2003 Dec; 123A(3):236-42. PubMed ID: 14608643
[TBL] [Abstract][Full Text] [Related]
10. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Johnston JJ; Olivos-Glander I; Killoran C; Elson E; Turner JT; Peters KF; Abbott MH; Aughton DJ; Aylsworth AS; Bamshad MJ; Booth C; Curry CJ; David A; Dinulos MB; Flannery DB; Fox MA; Graham JM; Grange DK; Guttmacher AE; Hannibal MC; Henn W; Hennekam RC; Holmes LB; Hoyme HE; Leppig KA; Lin AE; Macleod P; Manchester DK; Marcelis C; Mazzanti L; McCann E; McDonald MT; Mendelsohn NJ; Moeschler JB; Moghaddam B; Neri G; Newbury-Ecob R; Pagon RA; Phillips JA; Sadler LS; Stoler JM; Tilstra D; Walsh Vockley CM; Zackai EH; Zadeh TM; Brueton L; Black GC; Biesecker LG
Am J Hum Genet; 2005 Apr; 76(4):609-22. PubMed ID: 15739154
[TBL] [Abstract][Full Text] [Related]
11. Point mutations in human GLI3 cause Greig syndrome.
Wild A; Kalff-Suske M; Vortkamp A; Bornholdt D; König R; Grzeschik KH
Hum Mol Genet; 1997 Oct; 6(11):1979-84. PubMed ID: 9302279
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.
Brueton L; Huson SM; Winter RM; Williamson R
Am J Med Genet; 1988 Dec; 31(4):799-804. PubMed ID: 3239571
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Point mutations and deletions in the znfn1a1/ikaros gene in chemically induced murine lymphomas.
Karlsson A; Söderkvist P; Zhuang SM
Cancer Res; 2002 May; 62(9):2650-3. PubMed ID: 11980663
[TBL] [Abstract][Full Text] [Related]
15. A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene.
Hui CC; Joyner AL
Nat Genet; 1993 Mar; 3(3):241-6. PubMed ID: 8387379
[TBL] [Abstract][Full Text] [Related]
16. Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).
Vortkamp A; Franz T; Gessler M; Grzeschik KH
Mamm Genome; 1992; 3(8):461-3. PubMed ID: 1322743
[No Abstract] [Full Text] [Related]
17. Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
Kalff-Suske M; Wild A; Topp J; Wessling M; Jacobsen EM; Bornholdt D; Engel H; Heuer H; Aalfs CM; Ausems MG; Barone R; Herzog A; Heutink P; Homfray T; Gillessen-Kaesbach G; König R; Kunze J; Meinecke P; Müller D; Rizzo R; Strenge S; Superti-Furga A; Grzeschik KH
Hum Mol Genet; 1999 Sep; 8(9):1769-77. PubMed ID: 10441342
[TBL] [Abstract][Full Text] [Related]
18. Expanded mutational spectrum of the GLI3 gene substantiates genotype-phenotype correlations.
Jamsheer A; Sowińska A; Trzeciak T; Jamsheer-Bratkowska M; Geppert A; Latos-Bieleńska A
J Appl Genet; 2012 Nov; 53(4):415-22. PubMed ID: 22903559
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
