290 related articles for article (PubMed ID: 20201963)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote.
Kariminejad A; Ghaderi-Sohi S; Keshavarz E; Hashemi SA; Parsimehr E; Szenker-Ravi E; Khatoo M; Faraji Zonooz M; Reversade B; Najmabadi H; Hennekam RC
Clin Genet; 2020 Jun; 97(6):915-919. PubMed ID: 32112393
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Exencephaly induction by valproic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.
Maekawa M; Ohta K; Katagiri R; Ueta E; Naruse I
Congenit Anom (Kyoto); 2005 Dec; 45(4):132-6. PubMed ID: 16359493
[TBL] [Abstract][Full Text] [Related]
13. Gli3 expression is affected in the morphogenetic mouse mutants add and Xt.
Schimmang T; van der Hoeven F; Rüther U
Prog Clin Biol Res; 1993; 383A():153-61. PubMed ID: 8302891
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas.
Ito S; Kitazawa R; Haraguchi R; Kondo T; Ouchi A; Ueda Y; Kitazawa S
Diagn Pathol; 2018 Jan; 13(1):1. PubMed ID: 29368652
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex.
Volodarsky M; Langer Y; Birk OS
BMC Med Genet; 2014 Sep; 15():110. PubMed ID: 25267529
[TBL] [Abstract][Full Text] [Related]
18. Genetic susceptibility in the neural tube defects induced by ochratoxin A in the genetic arhinencephaly mouse, Pdn/Pdn.
Ohta K; Maekawa M; Katagiri R; Ueta E; Naruse I
Congenit Anom (Kyoto); 2006 Sep; 46(3):144-8. PubMed ID: 16922921
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. High-resolution mapping of the Gli3 deletion in the mouse extra-toesH mutant.
Genestine M; Robert B; Lallemand Y
Genesis; 2007 Mar; 45(3):107-12. PubMed ID: 17304534
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
