128 related articles for article (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; 50(4):388-90. PubMed ID: 8209924
[TBL] [Abstract][Full Text] [Related]
2. Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27.
Xuan JY; Besner A; Ireland M; Hughes-Benzie RM; MacKenzie AE
Hum Mol Genet; 1994 Jan; 3(1):133-7. PubMed ID: 7909248
[TBL] [Abstract][Full Text] [Related]
3. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
Lin AE
Am J Med Genet; 1993 Jun; 46(5):606-7. PubMed ID: 8322829
[No Abstract] [Full Text] [Related]
4. Simpson-Golabi-Behmel syndrome (SGBS) in a female with an X-autosome translocation.
Punnett HH
Am J Med Genet; 1994 May; 50(4):391-3. PubMed ID: 8209925
[No Abstract] [Full Text] [Related]
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; 34(4):470-4. PubMed ID: 2624254
[TBL] [Abstract][Full Text] [Related]
6. The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
Gelernter J; Vandenbergh D; Kruger SD; Pauls DL; Kurlan R; Pakstis AJ; Kidd KK; Uhl G
Genomics; 1995 Dec; 30(3):459-63. PubMed ID: 8825631
[TBL] [Abstract][Full Text] [Related]
7. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
Gurrieri F; Cappa M; Neri G
Am J Med Genet; 1992 Sep; 44(2):136-7. PubMed ID: 1456280
[TBL] [Abstract][Full Text] [Related]
8. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.
Stanier P; Forbes SA; Arnason A; Bjornsson A; Sveinbjornsdottir E; Williamson R; Moore G
Genomics; 1993 Sep; 17(3):549-55. PubMed ID: 8244369
[TBL] [Abstract][Full Text] [Related]
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; 16(1):259-61. PubMed ID: 8486368
[TBL] [Abstract][Full Text] [Related]
10. [Simpson-Golabi-Behmel syndrome].
Kubota T
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):638-9. PubMed ID: 11528938
[No Abstract] [Full Text] [Related]
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; 12(3):241-7. PubMed ID: 8589713
[TBL] [Abstract][Full Text] [Related]
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; 50(10):1106-8. PubMed ID: 11712343
[TBL] [Abstract][Full Text] [Related]
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; 41(1):93-9. PubMed ID: 9126487
[TBL] [Abstract][Full Text] [Related]
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; 220(3):824-7. PubMed ID: 8607849
[TBL] [Abstract][Full Text] [Related]
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; 73(1):87-90. PubMed ID: 9375929
[TBL] [Abstract][Full Text] [Related]
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; 49(4):431-4. PubMed ID: 7909197
[TBL] [Abstract][Full Text] [Related]
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; 44(2):129-35. PubMed ID: 1456279
[TBL] [Abstract][Full Text] [Related]
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; 45(4):163-7. PubMed ID: 8355647
[TBL] [Abstract][Full Text] [Related]
19. Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.
Turner G; Gedeon A; Mulley J; Sutherland G; Rae J; Power K; Arthur I
Am J Med Genet; 1989 Dec; 34(4):463-9. PubMed ID: 2624253
[TBL] [Abstract][Full Text] [Related]
20. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.
Robin NH; Feldman GJ; Aronson AL; Mitchell HF; Weksberg R; Leonard CO; Burton BK; Josephson KD; Laxová R; Aleck KA; Allanson JE; Guion-Almeida ML; Martin RA; Leichtman LG; Price RA; Opitz JM; Muenke M
Nat Genet; 1995 Dec; 11(4):459-61. PubMed ID: 7493033
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]