Bone marrow failure in Shwachman-Diamond syndrome does not select for clonal haematopoiesis of the paroxysmal nocturnal haemoglobinuria phenotype

British Journal of Haematology

Volumn 119, Issue 3, 2002, Pages 830-832

  Keller, Peter ^a   Debaun, Michael R ^a   Rothbaum, Robert J ^a   Bessler, Monica ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Bone marrow failure; Glycosyl phosphatidylinositol (GPI) linked proteins; Paroxysmal nocturnal haemoglobinuria (PNH); Shwachman Diamond Syndrome (SDS)

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BLOOD CELL; BONE MARROW DEPRESSION; CHILD; CLINICAL ARTICLE; CLONAL VARIATION; CONTROLLED STUDY; FEMALE; HEMATOPOIESIS; HUMAN; MALE; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PHENOTYPE; PRIORITY JOURNAL; SHWACHMAN SYNDROME; STEM CELL;

ADOLESCENT; ADULT; ANEMIA, DIAMOND-BLACKFAN; CHILD; CLONE CELLS; FEMALE; HEMATOPOIESIS; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; MALE; PHENOTYPE;

EID: 0036434943     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.03913.x     Document Type: Article

References (12)

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