BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 8974918)

  • 1. [Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].
    Nemtsova MV; Iatsenko AN; Kuleshov NP; Novikov PV; Meerson EM; Zaletaev DV
    Genetika; 1996 Jul; 32(7):978-84. PubMed ID: 8974918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning the BOR gene.
    Gu JZ; Wagner MJ; Haan EA; Wells DE
    Genomics; 1996 Jan; 31(2):201-6. PubMed ID: 8824802
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.
    Momeni P; Glöckner G; Schmidt O; von Holtum D; Albrecht B; Gillessen-Kaesbach G; Hennekam R; Meinecke P; Zabel B; Rosenthal A; Horsthemke B; Lüdecke HJ
    Nat Genet; 2000 Jan; 24(1):71-4. PubMed ID: 10615131
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tricho-rhino-phalangeal syndrome type II (Langer-Giedion) with persistent cloaca and prune belly sequence in a girl with 8q interstitial deletion.
    Ramos FJ; McDonald-McGinn DM; Emanuel BS; Zackai EH
    Am J Med Genet; 1992 Dec; 44(6):790-4. PubMed ID: 1481848
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tricho-rhino-phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24.
    Marchau FE; Van Roy BC; Parizel PM; Lambert JR; De Canck I; Leroy JG; Gevaert CM; Willems PJ; Dumon JE
    Am J Med Genet; 1993 Feb; 45(4):450-5. PubMed ID: 8465849
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A final word on the tricho-rhino-phalangeal syndromes.
    Bühler EM; Bühler UK; Beutler C; Fessler R
    Clin Genet; 1987 Apr; 31(4):273-5. PubMed ID: 3594935
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.
    Bowen P; Biederman B; Hoo JJ
    Ann Genet; 1985; 28(4):224-7. PubMed ID: 3879433
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome.
    Hilton MJ; Gutiérrez L; Zhang L; Moreno PA; Reddy M; Brown N; Tan Y; Hill A; Wells DE
    Genomics; 2001 Jan; 71(2):192-9. PubMed ID: 11161813
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU; Baumann WA
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Langer-Giedion syndrome(tricho-rhino-phalangeal syndrome, type II; TRPS II)].
    Fukushima Y
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):203-4. PubMed ID: 11057196
    [No Abstract]   [Full Text] [Related]  

  • 11. Integrity of the thyroglobulin locus in tricho-rhino-phalangeal syndrome II.
    Brocas H; Bühler EM; Simon P; Malik NJ; Vassart G
    Hum Genet; 1986 Oct; 74(2):178-80. PubMed ID: 2876948
    [TBL] [Abstract][Full Text] [Related]  

  • 12. BMP-1 sublocalization on human chromosome 8. Molecular anatomy and orthopaedic implications.
    Shore EM; Cook AL; Hahn GV; Kaplan FS; Wozney JM; Wagner MJ; Wells DE
    Clin Orthop Relat Res; 1995 Feb; (311):199-209. PubMed ID: 7634576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions.
    Nardmann J; Tranebjaerg L; Horsthemke B; Lüdecke HJ
    Hum Genet; 1997 May; 99(5):638-43. PubMed ID: 9150732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.
    Verheij JB; de Munnik SA; Dijkhuizen T; de Leeuw N; Olde Weghuis D; van den Hoek GJ; Rijlaarsdam RS; Thomasse YE; Dikkers FG; Marcelis CL; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2009; 52(5):353-7. PubMed ID: 19464398
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.
    Lüdecke HJ; Wagner MJ; Nardmann J; La Pillo B; Parrish JE; Willems PJ; Haan EA; Frydman M; Hamers GJ; Wells DE
    Hum Mol Genet; 1995 Jan; 4(1):31-6. PubMed ID: 7711731
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prometaphase chromosomes in the tricho-rhino-phalangeal syndrome type I.
    Yamamoto Y; Oguro N; Miyao M; Yanagisawa M; Ohsawa T
    Am J Med Genet; 1989 Apr; 32(4):524-7. PubMed ID: 2773997
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1).
    Ahn J; Lüdecke HJ; Lindow S; Horton WA; Lee B; Wagner MJ; Horsthemke B; Wells DE
    Nat Genet; 1995 Oct; 11(2):137-43. PubMed ID: 7550340
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel TRPS1 mutation in a family with tricho-rhino-phalangeal syndrome type 1.
    Fujisawa T; Fukao T; Shimomura Y; Seishima M
    J Dermatol; 2014 Jun; 41(6):514-7. PubMed ID: 24909213
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy.
    Fryns JP; Emmery L; Timmermans J; Pedersen JC; van den Berghe H
    J Genet Hum; 1980 Mar; 28(1):53-6. PubMed ID: 7400785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletion.
    Tiberio G; Digilio MC; Giannotti A
    Minerva Pediatr; 1999; 51(9-10):313-8. PubMed ID: 10783592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.