83 related articles for article (PubMed ID: 3232706)
1. Genetic prediction in X-linked agammaglobulinaemia.
Lau YL; Levinsky RJ; Malcolm S; Goodship J; Winter R; Pembrey M
Am J Med Genet; 1988 Oct; 31(2):437-48. PubMed ID: 3232706
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Carrier detection for X-linked agammaglobulinaemia (Bruton type) in an Irish family using linked DNA probes.
Reardon W; Genet S; Middleton-Price H; Malcolm S; Feighery C
Ir Med J; 1991 Dec-1992 Jan; 84(4):116-8. PubMed ID: 1817116
[TBL] [Abstract][Full Text] [Related]
4. Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.
Parolini O; Hejtmancik JF; Allen RC; Belmont JW; Lassiter GL; Henry MJ; Barker DF; Conley ME
Genomics; 1993 Feb; 15(2):342-9. PubMed ID: 8449500
[TBL] [Abstract][Full Text] [Related]
5. Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.
Journet O; Durandy A; Doussau M; Le Deist F; Couvreur J; Griscelli C; Fischer A; de Saint-Basile G
Am J Med Genet; 1992 Jul; 43(5):885-7. PubMed ID: 1642281
[TBL] [Abstract][Full Text] [Related]
6. Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.
Guioli S; Arveiler B; Bardoni B; Notarangelo LD; Panina P; Duse M; Ugazio A; Oberlé I; de Saint Basile G; Mandel JL
Hum Genet; 1989 Dec; 84(1):19-21. PubMed ID: 2575070
[TBL] [Abstract][Full Text] [Related]
7. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.
Kwan SP; Terwilliger J; Parmley R; Raghu G; Sandkuyl LA; Ott J; Ochs H; Wedgwood R; Rosen F
Genomics; 1990 Feb; 6(2):238-42. PubMed ID: 2307467
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Additional polymorphisms useful in linkage analysis for X-linked agammaglobulinemia.
Parolini O; Conley ME
Immunodeficiency; 1993; 4(1-4):217-9. PubMed ID: 8167704
[No Abstract] [Full Text] [Related]
10. 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]
11. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.
Schrander-Stumpel C; Meyer H; Merckx D; Jones M; Israel J; Sommer A; Stevens C; Tinschert S; Wilson G; Willems P
Genet Couns; 1994; 5(1):1-10. PubMed ID: 8031529
[TBL] [Abstract][Full Text] [Related]
12. DNA probes in X-linked retinitis pigmentosa.
Wright AF; Bhattacharya S; Price WH; Phillips CI; McKeown C; Crews SJ; Jay M; Bird AC
Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 4)():467-74. PubMed ID: 6589864
[TBL] [Abstract][Full Text] [Related]
13. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.
Andrews DF; Brasher PM; Manchester KE; Percy ME; Rusk AC; Soltan HC; Trueman DW
Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018
[TBL] [Abstract][Full Text] [Related]
14. Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
Hinds H; Craig IW; Chen ZY; Kraakman ME; Schuurman RK; Hendriks RW
Immunodeficiency; 1993; 4(1-4):213-5. PubMed ID: 8167703
[TBL] [Abstract][Full Text] [Related]
15. Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
Vorechovský I; Holland J; Sideras P; Dunham I; Hammarström L; Smith CI; Bentley DR; Vetrie D
Immunodeficiency; 1993; 4(1-4):221-4. PubMed ID: 8167705
[TBL] [Abstract][Full Text] [Related]
16. Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
Hendriks RW; Chen ZY; Hinds H; Schuurman RK; Craig IW
Immunodeficiency; 1993; 4(1-4):209-11. PubMed ID: 8167702
[TBL] [Abstract][Full Text] [Related]
17. Expression of the gene defect in X-linked agammaglobulinemia.
Conley ME; Brown P; Pickard AR; Buckley RH; Miller DS; Raskind WH; Singer JW; Fialkow PJ
N Engl J Med; 1986 Aug; 315(9):564-7. PubMed ID: 3488506
[No Abstract] [Full Text] [Related]
18. Early diagnosis in X-linked agammaglobulinaemia.
Schuurman RK; Mensink EJ; Sandkuyl LA; Post ED; van Velzen-Blad H
Eur J Pediatr; 1988 Jan; 147(1):93-5. PubMed ID: 2892683
[TBL] [Abstract][Full Text] [Related]
19. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.
Vetrie D; Vorechovský I; Sideras P; Holland J; Davies A; Flinter F; Hammarström L; Kinnon C; Levinsky R; Bobrow M
Nature; 1993 Jan; 361(6409):226-33. PubMed ID: 8380905
[TBL] [Abstract][Full Text] [Related]
20. Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy.
Williams WR; Thompson MW; Morton NE
Am J Med Genet; 1983 Feb; 14(2):315-33. PubMed ID: 6837627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
