A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.

Lin, Q; Rohrer, J; Allen, R C; Larché, M; Greene, J M; Shigeoka, A O; Gatti, R A; Derauf, D C; Belmont, J W; Conley, M E

Lin, Q; Rohrer, J; Allen, R C; Larché, M; Greene, J M; Shigeoka, A O; Gatti, R A; Derauf, D C; Belmont, J W; Conley, M E.

Affiliation

Lin Q; Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

J Clin Invest ; 97(1): 196-201, 1996 Jan 01.

Article in En | MEDLINE | ID: mdl-8550833

Subject(s)

DNA Mutational Analysis; Hypergammaglobulinemia/genetics; Immunoglobulin M; Membrane Glycoproteins/genetics; Polymorphism, Single-Stranded Conformational; X Chromosome; Base Sequence; CD40 Ligand; Child; Child, Preschool; DNA Primers/genetics; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Infant; Lymphocyte Activation; Male; Molecular Sequence Data; Pedigree; Polymerase Chain Reaction/methods; Syndrome; T-Lymphocytes/chemistry; T-Lymphocytes/immunology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Immunoglobulin M / DNA Mutational Analysis / Membrane Glycoproteins / Polymorphism, Single-Stranded Conformational / Hypergammaglobulinemia Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Clin Invest Year: 1996 Type: Article Affiliation country: United States

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