Comprehensive genetic testing for primary immunodeficiency disorders in a tertiary hospital: 10-year experience in Auckland, New Zealand

Allergy, Asthma and Clinical Immunology

Volumn 12, Issue 1, 2016, Pages

  Woon, See Tarn ^a   Ameratunga, Rohan ^a  

^a AUCKLAND CITY HOSPITAL   (New Zealand)

Author keywords

Genetic testing; Next generation sequencing; Primary immunodeficiencies

Indexed keywords

AGAMMAGLOBULINEMIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; B LYMPHOCYTE; CONGENITAL DISORDER OF GLYCOSYLATION; ECTODERMAL DYSPLASIA; FEMALE; GENE LOCUS; GENETIC COUNSELING; GENETIC SCREENING; GRISCELLI SYNDROME; HEMOPHAGOCYTIC SYNDROME; HETEROZYGOTE; HUMAN; IMMUNE DEFICIENCY; LYMPHOPROLIFERATIVE DISEASE; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NEW ZEALAND; NEXT GENERATION SEQUENCING; SHWACHMAN SYNDROME; TERTIARY CARE CENTER; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED PERIODIC SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 85002033467     PISSN: 17101484     EISSN: 17101492     Source Type: Journal    
DOI: 10.1186/s13223-016-0169-2     Document Type: Article

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