Congenital thrombocytopenia and radio-ulnar synostosis: A new familial syndrome

British Journal of Haematology

Volumn 113, Issue 4, 2001, Pages 866-870

  Thompson, Alexis A ^a,b   Woodruff, Kelly ^a   Feig, Stephen A ^a   Nguyen, Long T ^a   Carolyn Schanen, N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CHILDREN'S MEMORIAL HOSPITAL   (United States)

Author keywords

Amegakaryocytic thrombocytopenia; Marrow failure; Radio ulnar synostosis; Skeletal defects; Thrombocytopenia

Indexed keywords

AMEGAKARYOCYTIC THROMBOCYTOPENIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE MARROW DEPRESSION; CASE REPORT; CHILD; CLINICAL FEATURE; COMORBIDITY; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; FAMILY STUDY; FANCONI ANEMIA; FEMALE; HUMAN; INFANT; MALE; MOLECULAR GENETICS; PRIORITY JOURNAL; RADIOULNAR SYNOSTOSIS; RADIUS APLASIA; SKELETON MALFORMATION; SYNOSTOSIS; THROMBOCYTOPENIA; THROMBOCYTOPENIA ABSENT RADIUS;

BONE MARROW CELLS; CHILD, PRESCHOOL; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MEGAKARYOCYTES; PEDIGREE; RADIUS; SYNDROME; SYNOSTOSIS; THROMBOCYTOPENIA; ULNA;

EID: 0034936465     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2001.02834.x     Document Type: Article

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