177 related articles for article (PubMed ID: 11057130)
1. [Pallister-Hall syndrome].
Oho Y; Okuyama T
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):23-5. PubMed ID: 11057130
[No Abstract] [Full Text] [Related]
2. [Hall syndrome (Pallister-Hall syndrome)].
Kuniba H; Egashira M; Motomura H; Motomura K; Kondoh T
Nihon Rinsho; 2006 Sep; Suppl 3():591-3. PubMed ID: 17022615
[No 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. [Greig cephalopolysyndactyly syndrome].
Satokata I
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):184-6. PubMed ID: 11057189
[No Abstract] [Full Text] [Related]
5. Pallister-Hall syndrome phenotype in mice mutant for Gli3.
Böse J; Grotewold L; Rüther U
Hum Mol Genet; 2002 May; 11(9):1129-35. PubMed ID: 11978771
[TBL] [Abstract][Full Text] [Related]
6. Gene symbol: GLI3. Disease: Pallister-Hall syndrome.
Kalff-Suske M; Paparidis Z; Bornholdt D; Cole T; Kalff-Suske M; Grzeschik KH
Hum Genet; 2004 Mar; 114(4):403. PubMed ID: 15046066
[No Abstract] [Full Text] [Related]
7. Autosomal dominant transmission of Pallister-Hall syndrome.
Penman Splitt M; Wright C; Perry R; Burn J
Clin Dysmorphol; 1994 Oct; 3(4):301-8. PubMed ID: 7894735
[TBL] [Abstract][Full Text] [Related]
8. Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis.
Killoran CE; Abbott M; McKusick VA; Biesecker LG
Clin Genet; 2000 Jul; 58(1):28-30. PubMed ID: 10945658
[TBL] [Abstract][Full Text] [Related]
9. Familial Pallister-Hall syndrome: case report and hormonal evaluation.
Sills IN; Rapaport R; Robinson LP; Lieber C; Shih LY; Horlick MN; Schwartz M; Desposito F
Am J Med Genet; 1993 Sep; 47(3):321-5. PubMed ID: 8135274
[TBL] [Abstract][Full Text] [Related]
10. Pallister-Hall syndrome with stenosis of the cricoid cartilage and microphallus without hypopituitarism.
Stoll C; De Saint Martin A; Donato L; Alembik K; Sauvage P; Messer J
Genet Couns; 2001; 12(3):231-5. PubMed ID: 11693785
[TBL] [Abstract][Full Text] [Related]
11. Gene symbol: GLI3. Disease: Pallister-Hall syndrome.
Freese K; Driess S; Bornholdt D; Shoenle EJ; Seidel H; Tinschert S; Grzeschik KH; Kalff-Suske M
Hum Genet; 2003 Jan; 112(1):103. PubMed ID: 12575661
[No Abstract] [Full Text] [Related]
12. Gli 3 mutation in Pallister-Hall syndrome.
Stoll C; De Saint Martin A; Donato L; Alembik Y; Sauvage P; Messer J
Genet Couns; 2002; 13(1):69. PubMed ID: 12017244
[No Abstract] [Full Text] [Related]
13. Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome.
Kang S; Allen J; Graham JM; Grebe T; Clericuzio C; Patronas N; Ondrey F; Green E; Schäffer A; Abbott M; Biesecker LG
J Med Genet; 1997 Jun; 34(6):441-6. PubMed ID: 9192261
[TBL] [Abstract][Full Text] [Related]
14. Mutation in GLI3 in postaxial polydactyly type A.
Radhakrishna U; Wild A; Grzeschik KH; Antonarakis SE
Nat Genet; 1997 Nov; 17(3):269-71. PubMed ID: 9354785
[No Abstract] [Full Text] [Related]
15. Long-term treatment with growth hormone improves final height in a patient with Pallister-Hall syndrome.
Galasso C; Scirè G; Fabbri F; Spadoni GL; Killoran CE; Biesecker LG; Boscherini B
Am J Med Genet; 2001 Mar; 99(2):128-31. PubMed ID: 11241471
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Total colonic aganglionosis and imperforate anus in a severely affected infant with Pallister-Hall syndrome.
Li MH; Eberhard M; Mudd P; Javia L; Zimmerman R; Khalek N; Zackai EH
Am J Med Genet A; 2015 Mar; 167A(3):617-20. PubMed ID: 25604768
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations.
Hall JG; Pallister PD; Clarren SK; Beckwith JB; Wiglesworth FW; Fraser FC; Cho S; Benke PJ; Reed SD
Am J Med Genet; 1980; 7(1):47-74. PubMed ID: 7211952
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]