Autoinflammatory Gene Panel Mayo Clinic Laboratories Mayo Clinic
United States | 182 | 117 | - C Sequence analysis of the entire coding region
|
Bcell/Antibody Deficiency GenePanel Mayo Clinic Laboratories Mayo Clinic
United States | 79 | 61 | - C Sequence analysis of the entire coding region
|
IKBKG - Sanger sequencing Centogene AG - the Rare Disease Company
Germany | 4 | 1 | - C Sequence analysis of the entire coding region
|
Mendelian Susceptibility to Mycobacterial Disease Panel PreventionGenetics, part of Exact Sciences
United States | 29 | 17 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Invasive pneumococcal disease, recurrent isolated, 2, 300640; IPD2 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Invasive pneumococcal disease, recurrent isolated, 2, 300640; IPD2 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Congenital Diarrhea and Enteropathies Panel PreventionGenetics, part of Exact Sciences
United States | 241 | 157 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences
United States | 191 | 141 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Incontinentia Pigmenti Common Deletion Analysis (Prenatal Diagnosis) Baylor Genetics
United States | 4 | 1 | - T Targeted variant analysis
|
Incontinentia Pigmenti Common Deletion Analysis Baylor Genetics
United States | 4 | 1 | - T Targeted variant analysis
|
X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States | 240 | 171 | - D Deletion/duplication analysis
|
IKBKG Institute for Human Genetics University Medical Center Freiburg
Germany | 3 | 1 | - C Sequence analysis of the entire coding region
|
