Clinical application of DNA microarrays: Molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency

Clinical Immunology

Volumn 128, Issue 1, 2008, Pages 31-38

  Strauss, Kevin A ^a,b,c   Puffenberger, Erik G ^a,b   Bunin, Nancy ^d   Rider, Nicholas L ^e   Morton, Mary C ^a   Eastman III, James T ^c   Morton, D Holmes ^a,b,c  

^a CLINIC FOR SPECIAL CHILDREN   (United States)

^b FRANKLIN AND MARSHALL COLLEGE   (United States)

^c LANCASTER GENERAL HOSPITAL   (United States)

^d CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^e PENN STATE COLLEGE OF MEDICINE   (United States)

Author keywords

HLA matching; Molecular biology; Omenn syndrome; Severe combined immune deficiency; Transplantation

Indexed keywords

ADENINE; BUSULFAN; CORTICOSTEROID; CYCLOPHOSPHAMIDE; CYCLOSPORIN; GUANINE; RECOMBINASE; TACROLIMUS; THYMOCYTE ANTIBODY;

ALOPECIA; ARTICLE; BONE MARROW TRANSPLANTATION; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC VALUE; DNA MICROARRAY; ERYTHRODERMA; FEMALE; FOLLOW UP; GENE; GENE SEQUENCE; GENOTYPE; GRAFT VERSUS HOST REACTION; HEMOLYTIC ANEMIA; HEPATOSPLENOMEGALY; HLA MATCHING; HUMAN; HYPEREOSINOPHILIA; INFANT; LINKAGE ANALYSIS; PRIORITY JOURNAL; RAG1 GENE; RELIGION; SEQUENCE ANALYSIS; SEVERE COMBINED IMMUNODEFICIENCY; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM; STEM CELL TRANSPLANTATION; SYMPTOM;

BONE MARROW TRANSPLANTATION; FEMALE; GENES, RAG-1; GENOTYPE; HAPLOTYPES; HISTOCOMPATIBILITY TESTING; HLA ANTIGENS; HUMANS; INFANT; INFANT, NEWBORN; MOLECULAR DIAGNOSTIC TECHNIQUES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEVERE COMBINED IMMUNODEFICIENCY;

EID: 49949152171     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2008.02.016     Document Type: Article

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