Additional file 1: Table S1. Blood routine test findings of the children with XHIGM
The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders resulting...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
Information on known pathogenic or expected pathogenic variants according to the ACMG reportable gen...
Hyper IgM (HIGM) syndromes are a complex of primary immunodeficiency disorders. A 4-years-old boy wi...
Hyper-IgM syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by elevated or n...
Hyper-IgM syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by elevated or n...
Background: X-linked hyper-IgM syndrome (XHIGM) is a rare primary immunodeficiency caused by CD40 li...
X-linked hyper-IgM syndrome (XHIGM) is one type of primary immunodeficiency diseases, resulting from...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
syndrome in a family with multiple deaths of affected males All males in two generations of a Hungar...
X-linked hyper IgM syndrome (XHIM) is a primary immunode-ficiency disorder caused by mutations of th...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
Hyper-IgM syndrome is a rare combined immune deficiency linked to a mutation most frequently found i...
The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders resulting...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
Information on known pathogenic or expected pathogenic variants according to the ACMG reportable gen...
Hyper IgM (HIGM) syndromes are a complex of primary immunodeficiency disorders. A 4-years-old boy wi...
Hyper-IgM syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by elevated or n...
Hyper-IgM syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by elevated or n...
Background: X-linked hyper-IgM syndrome (XHIGM) is a rare primary immunodeficiency caused by CD40 li...
X-linked hyper-IgM syndrome (XHIGM) is one type of primary immunodeficiency diseases, resulting from...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
syndrome in a family with multiple deaths of affected males All males in two generations of a Hungar...
X-linked hyper IgM syndrome (XHIM) is a primary immunode-ficiency disorder caused by mutations of th...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
Hyper-IgM syndrome is a rare combined immune deficiency linked to a mutation most frequently found i...
The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders resulting...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
Information on known pathogenic or expected pathogenic variants according to the ACMG reportable gen...
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