Pages that link to "Q57635557"

The following pages link to Molecular diagnosis of X-linked agammaglobulinaemia (Q57635557):

Displaying 13 items.

• Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA) (Q30194173) (← links)
• Identification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemia (Q33678961) (← links)
• Kinase mutations in human disease: interpreting genotype-phenotype relationships (Q34088851) (← links)
• Mutations in btk in patients with presumed X-linked agammaglobulinemia (Q34385386) (← links)
• Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site. (Q35238731) (← links)
• The PAX5 gene: a linkage and mutation analysis in candidate human primary immunodeficiencies (Q38300712) (← links)
• Molecular and cellular aspects of X-linked agammaglobulinemia. (Q40373279) (← links)
• X-linked agammaglobulinemia and other immunoglobulin deficiencies (Q40694868) (← links)
• B-cell-specific demethylation of BTK, the defective gene in X-linked agammaglobulinemia (Q41403536) (← links)
• Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed? (Q57734381) (← links)
• Molecular basis for X-linked immunodeficiencies (Q73827686) (← links)
• [Common variable immunodeficiency in children] (Q77752927) (← links)
• Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency (Q98499845) (← links)