Absence of mutations in the HoxA10, HoxA11 and HoxD11 nucleotide coding sequences in thrombocytopenia with absent radius syndrome

British Journal of Haematology

Volumn 116, Issue 2, 2002, Pages 367-375

  Fleischman, Roger A ^a   Mi, Xiafang ^a   Stevens, David ^a   Winters, Jeffrey ^a   Letestu, Rémi ^b   Debili, Najet ^b   Vainchenker, William ^b  

^a UNIVERSITY OF KENTUCKY   (United States)

^b INSTITUT GUSTAVE ROUSSY   (France)

Author keywords

Homeobox genes; Limb deformity; Megakaryocytes; Radius; Thrombocytopenia

Indexed keywords

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ARTICLE; BONE DEVELOPMENT; BONE MARROW CELL; CELL LINE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE; GENE AMPLIFICATION; GENE DELETION; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; GENE REARRANGEMENT; GENETIC TRANSCRIPTION; HOXA10 GENE; HOXA11 GENE; HOXD11 GENE; HUMAN; HUMAN CELL; MALE; MEGAKARYOCYTE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RADIUS APLASIA; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOUTHERN BLOTTING; THROMBOCYTOPENIA; UMBILICAL CORD BLOOD;

ADOLESCENT; ADULT; BLOTTING, NORTHERN; CELL LINE; CHILD; CHILD, PRESCHOOL; FEMALE; FETAL BLOOD; GENES, HOMEOBOX; HUMANS; MALE; MEGAKARYOCYTES; MIDDLE AGED; MUTATION; RADIUS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SYNDROME; THROMBOCYTOPENIA;

EID: 0036175014     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.03263.x     Document Type: Article

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