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Journal Abstract Search

124 related items for PubMed ID: 8209924

  • 1. Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European families.
    Orth U, Gurrieri F, Behmel A, Genuardi M, Cremer M, Gal A, Neri G.
    Am J Med Genet; 1994 May 01; 50(4):388-90. PubMed ID: 8209924
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  • 3. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Lin AE.
    Am J Med Genet; 1993 Jun 15; 46(5):606-7. PubMed ID: 8322829
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  • 5. Linkage localization of Börjeson-Forssman-Lehmann syndrome.
    Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA.
    Am J Med Genet; 1989 Dec 15; 34(4):470-4. PubMed ID: 2624254
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  • 9. Genetic mapping of X-linked ocular albinism: linkage analysis in a large Newfoundland kindred.
    Charles SJ, Green JS, Moore AT, Barton DE, Yates JR.
    Genomics; 1993 Apr 15; 16(1):259-61. PubMed ID: 8486368
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  • 10. [Simpson-Golabi-Behmel syndrome].
    Kubota T.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 15; (34 Pt 2):638-9. PubMed ID: 11528938
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  • 11. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.
    Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D.
    Nat Genet; 1996 Mar 15; 12(3):241-7. PubMed ID: 8589713
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  • 12. [Anesthetic management in a patient with Simpson-Golabi-Behmel syndrome].
    Tsuchiya K, Takahata O, Sengoku K, Hamada I, Suzuki A, Iwasaki H.
    Masui; 2001 Oct 15; 50(10):1106-8. PubMed ID: 11712343
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  • 13. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF.
    Genomics; 1997 Apr 01; 41(1):93-9. PubMed ID: 9126487
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  • 14. Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.
    Shastry BS, Hejtmancik FJ, Margherio RT, Trese MT.
    Biochem Biophys Res Commun; 1996 Mar 27; 220(3):824-7. PubMed ID: 8607849
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  • 15. A gene for FG syndrome maps in the Xq12-q21.31 region.
    Briault S, Hill R, Shrimpton A, Zhu D, Till M, Ronce N, Margaritte-Jeannin P, Baraitser M, Middleton-Price H, Malcolm S, Thompson E, Hoo J, Wilson G, Romano C, Guichet A, Pembrey M, Fontes M, Poustka A, Moraine C.
    Am J Med Genet; 1997 Nov 28; 73(1):87-90. PubMed ID: 9375929
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  • 16. Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26.
    Parvari R, Weinstein Y, Ehrlich S, Steinitz M, Carmi R.
    Am J Med Genet; 1994 Feb 15; 49(4):431-4. PubMed ID: 7909197
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  • 17. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.
    Garganta CL, Bodurtha JN.
    Am J Med Genet; 1992 Sep 15; 44(2):129-35. PubMed ID: 1456279
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  • 18. [The Simpson-Golabi-Behmel syndrome. The stages of a diagnostic procedure].
    Di Rocco M, Lignana E, Faraci M, Leveratto L, Borrone C.
    Minerva Pediatr; 1993 Apr 15; 45(4):163-7. PubMed ID: 8355647
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