Analysis of deletions in three McLeod patients: Exclusion of the XS locus from the Xp21.1-Xp21.2 region

European Journal of Immunogenetics

Volumn 27, Issue 1, 2000, Pages 29-33

  El Nemer, Wassim ^a   Colin, Yves ^a   Collec, Emmanuel ^a   Gane, Pierre ^a   Cartron, Jean Pierre ^a   Le Van Kim, Caroline ^a  

^a INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROCYTE ANTIGEN;

ARTICLE; BLOOD GROUP; CASE REPORT; CHROMOSOME 19; CHROMOSOME DELETION X; CHROMOSOME XP; CONTROLLED STUDY; EXON; HEMATOLOGIC DISEASE; HUMAN; HUMAN CELL; HYPERTRANSLUCENT LUNG; INTERSTITIAL CHROMOSOME DELETION; MALE; MARKER GENE; NEUROMUSCULAR DISEASE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

ALLELES; BLOOD GROUP ANTIGENS; BLOTTING, SOUTHERN; EXONS; FLOW CYTOMETRY; GENE DELETION; GENES, RECESSIVE; HEMATOPOIETIC SYSTEM; HUMANS; NEUROMUSCULAR DISEASES; POLYMERASE CHAIN REACTION; SYNDROME; X CHROMOSOME;

EID: 0033976115     PISSN: 09607420     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2370.2000.00188.x     Document Type: Article

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