Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay

Genetic Testing

Volumn 1, Issue 4, 1998, Pages 261-267

  Grant, Stephen G ^a   Reeger, Wendy ^b,c   Wenger, Sharon L ^b,d  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^c Armstrong Pediatrics   (United States)

^d WEST VIRGINIA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA; ATAXIA TELANGIECTASIA;

ALPHA FETOPROTEIN; GLYCOPHORIN; IMMUNOGLOBULIN G;

AGAMMAGLOBULINEMIA; ALLELE; ARTICLE; ATAXIA TELANGIECTASIA; BLOOD; BLOOD GROUP MNSS SYSTEM; CASE REPORT; CHROMOSOME ABERRATION; ERYTHROCYTE DISORDER; FEMALE; GENE DUPLICATION; GENETICS; HETEROZYGOSITY LOSS; HUMAN; KARYOTYPING; LYMPHOCYTE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; RESPIRATORY TRACT INFECTION; ULTRASTRUCTURE;

AGAMMAGLOBULINEMIA; ALLELES; ALPHA-FETOPROTEINS; ATAXIA TELANGIECTASIA; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; DNA MUTATIONAL ANALYSIS; ERYTHROCYTES, ABNORMAL; FEMALE; GENE DUPLICATION; GLYCOPHORIN; HUMANS; IMMUNOGLOBULIN G; KARYOTYPING; LOSS OF HETEROZYGOSITY; LYMPHOCYTES; MNSS BLOOD-GROUP SYSTEM; RESPIRATORY TRACT INFECTIONS;

EID: 0031292790     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/gte.1997.1.261     Document Type: Article

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