118 related articles for article (PubMed ID: 2896158)
1. X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17.
Ivens A; Moore GE; Chambers J; Arnason A; Jensson O; Bjornsson A; Williamson R
Hum Genet; 1988 Apr; 78(4):356-8. PubMed ID: 2896158
[TBL] [Abstract][Full Text] [Related]
2. The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.
Gorski SM; Adams KJ; Birch PH; Friedman JM; Goodfellow PJ
Am J Hum Genet; 1992 May; 50(5):1129-36. PubMed ID: 1570839
[TBL] [Abstract][Full Text] [Related]
3. Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.
Moore GE; Williamson R; Jensson O; Chambers J; Takakubo F; Newton R; Balacs MA; Ivens A
J Craniofac Genet Dev Biol; 1991; 11(4):372-6. PubMed ID: 1687471
[TBL] [Abstract][Full Text] [Related]
4. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
Lesko JG; Lewis RA; Nussbaum RL
Am J Hum Genet; 1987 Apr; 40(4):303-11. PubMed ID: 2883887
[TBL] [Abstract][Full Text] [Related]
5. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
Schwartz M; Yang HM; Niebuhr E; Rosenberg T; Page DC
Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
[TBL] [Abstract][Full Text] [Related]
6. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
Arveiler B; Oberlé I; Mandel JL
Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
[TBL] [Abstract][Full Text] [Related]
7. X-linked cleft palate and ankyloglossia in an Icelandic family.
Björnsson A; Arnason A; Tippet P
Cleft Palate J; 1989 Jan; 26(1):3-8. PubMed ID: 2563678
[TBL] [Abstract][Full Text] [Related]
8. Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.
Mensink EJ; Thompson A; Schot JD; Kraakman ME; Sandkuyl LA; Schuurman RK
Clin Genet; 1987 Feb; 31(2):91-6. PubMed ID: 2881637
[TBL] [Abstract][Full Text] [Related]
9. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.
Kwan SP; Kunkel L; Bruns G; Wedgwood RJ; Latt S; Rosen FS
J Clin Invest; 1986 Feb; 77(2):649-52. PubMed ID: 3003164
[TBL] [Abstract][Full Text] [Related]
10. Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.
Forbes SA; Richardson M; Brennan L; Arnason A; Bjornsson A; Campbell L; Moore G; Stanier P
Hum Genet; 1995 Mar; 95(3):342-6. PubMed ID: 7868130
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.
Oberlé I; Drayna D; Camerino G; White R; Mandel JL
Proc Natl Acad Sci U S A; 1985 May; 82(9):2824-8. PubMed ID: 2986139
[TBL] [Abstract][Full Text] [Related]
13. Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).
Malcolm S; de Saint Basile G; Arveiler B; Lau YL; Szabo P; Fischer A; Griscelli C; Debre M; Mandel JL; Callard RE
Hum Genet; 1987 Oct; 77(2):172-4. PubMed ID: 2888720
[TBL] [Abstract][Full Text] [Related]
14. Linkage of an X-chromosome cleft palate gene.
Moore GE; Ivens A; Chambers J; Farrall M; Williamson R; Page DC; Bjornsson A; Arnason A; Jensson O
Nature; 1987 Mar 5-11; 326(6108):91-2. PubMed ID: 2881212
[TBL] [Abstract][Full Text] [Related]
15. X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.
Mensink EJ; Thompson A; Sandkuyl LA; Kraakman ME; Schot JD; Espanol T; Schuurman RK
Hum Genet; 1987 May; 76(1):96-9. PubMed ID: 2883112
[TBL] [Abstract][Full Text] [Related]
16. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
Forbes SA; Brennan L; Richardson M; Coffey A; Cole CG; Gregory SG; Bentley DR; Mumm S; Moore GE; Stanier P
Genomics; 1996 Jan; 31(1):36-43. PubMed ID: 8808277
[TBL] [Abstract][Full Text] [Related]
17. Human gene mapping.
Williamson R
Ciba Found Symp; 1987; 130():3-13. PubMed ID: 3481697
[TBL] [Abstract][Full Text] [Related]
18. Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.
Gal A; Schinzel A; Orth U; Fraser NA; Mollica F; Craig IW; Kruse T; Mächler M; Neugebauer M; Bleeker-Wagemakers LM
Hum Genet; 1989 Mar; 81(4):315-8. PubMed ID: 2564836
[TBL] [Abstract][Full Text] [Related]
19. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.
Skare JC; Sullivan JL; Milunsky A
Hum Genet; 1989 Jul; 82(4):349-53. PubMed ID: 2567695
[TBL] [Abstract][Full Text] [Related]
20. Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.
Morgan SH; Cheshire JK; Wilson TM; MacDermot K; Crawfurd MA
Pediatr Nephrol; 1987 Jul; 1(3):536-9. PubMed ID: 2908672
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]