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63. Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice. de Weers M; Mensink RG; Kraakman ME; Schuurman RK; Hendriks RW Hum Mol Genet; 1994 Jan; 3(1):161-6. PubMed ID: 8162018 [TBL] [Abstract][Full Text] [Related]
67. Characterization of germline mutations of the gene encoding Bruton's tyrosine kinase in families with X-linked agammaglobulinemia. Hagemann TL; Rosen FS; Kwan SP Hum Mutat; 1995; 5(4):296-302. PubMed ID: 7627183 [TBL] [Abstract][Full Text] [Related]
68. Detection of a novel mutation in the SRC homology domain 2 (SH2) of Bruton's tyrosine kinase and direct female carrier evaluation in a family with X-linked agammaglobulinemia. Schuster V; Seidenspinner S; Kreth HW Am J Med Genet; 1996 May; 63(1):318-22. PubMed ID: 8723128 [TBL] [Abstract][Full Text] [Related]
69. Linkage analysis of a large pedigree with hereditary sideroblastic anaemia. Noble JS; Taylor GR; Losowsky MS; Hall R; Turner G; Mueller RF; Stewart AD J Med Genet; 1995 May; 32(5):389-92. PubMed ID: 7616548 [TBL] [Abstract][Full Text] [Related]
70. Carrier determination for X-linked agammaglobulinemia using X inactivation analysis of purified B cells. Alterman LA; de Alwis M; Genet S; Lovering R; Middleton-Price H; Morgan G; Jones A; Malcolm S; Levinsky RJ; Kinnon C J Immunol Methods; 1993 Nov; 166(1):111-6. PubMed ID: 8228281 [TBL] [Abstract][Full Text] [Related]
71. Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome. Goonewardena P; Sjöholm AG; Nilsson LA; Pettersson U Genomics; 1988 Feb; 2(2):115-8. PubMed ID: 2900806 [TBL] [Abstract][Full Text] [Related]
72. Choroideremia-locus maps between DXS3 and DXS11 on Xq. Gal A; Brunsmann F; Hogenkamp D; Rüther K; Ahlert D; Wienker TF; Hammerstein W; Pawlowitzki IH Hum Genet; 1986 Jun; 73(2):123-6. PubMed ID: 3755117 [TBL] [Abstract][Full Text] [Related]
73. Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1. Caggana M; Ashley GA; Desnick RJ; Eng CM Am J Med Genet; 1997 Aug; 71(3):329-35. PubMed ID: 9268104 [TBL] [Abstract][Full Text] [Related]
74. Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers. Yates JR; Goudie DR; Gillard EF; Aitken DA; Affara NA; Clayton JF; Tippett PA; Ferguson-Smith MA Genomics; 1987 Sep; 1(1):52-9. PubMed ID: 3478297 [TBL] [Abstract][Full Text] [Related]
75. X linked agammaglobulinaemia with a 'leaky' phenotype. Jones A; Bradley L; Alterman L; Tarlow M; Thompson R; Kinnon C; Morgan G Arch Dis Child; 1996 Jun; 74(6):548-9. PubMed ID: 8758136 [TBL] [Abstract][Full Text] [Related]
76. Further localization of X-linked hydrocephalus in the chromosomal region Xq28. Willems PJ; Vits L; Raeymaekers P; Beuten J; Coucke P; Holden JJ; Van Broeckhoven C; Warren ST; Sagi M; Robinson D Am J Hum Genet; 1992 Aug; 51(2):307-15. PubMed ID: 1642232 [TBL] [Abstract][Full Text] [Related]
77. Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: a nationwide study of Btk deficiency in Greece. Speletas M; Kanariou M; Kanakoudi-Tsakalidou F; Papadopoulou-Alataki E; Arvanitidis K; Pardali E; Constantopoulos A; Kartalis G; Vihinen M; Sideras P; Ritis K Scand J Immunol; 2001 Sep; 54(3):321-7. PubMed ID: 11555397 [TBL] [Abstract][Full Text] [Related]
78. Genetic linkage analysis places locus DXS250 between locus DXYS1 and locus DXS3 in Xq21.3. Epting S; Schwartz C Cytogenet Cell Genet; 1992; 60(2):112-3. PubMed ID: 1611908 [TBL] [Abstract][Full Text] [Related]
79. Refining the genetic location of the gene for X linked hydrocephalus within Xq28. Jouet M; Feldman E; Yates J; Donnai D; Paterson J; Siggers D; Kenwrick S J Med Genet; 1993 Mar; 30(3):214-7. PubMed ID: 8474107 [TBL] [Abstract][Full Text] [Related]
80. Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: further narrowing of the RS candidate region. Dumur V; Trivier E; Puech B; Peugnet F; Zanlonghi X; Hache JC; Hanauer A Hum Genet; 1995 Jul; 96(1):79-82. PubMed ID: 7607659 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]