An abnormal clone with monosomy 7 and trisomy 21 in the bone marrow of a child with congenital agranulocytosis (Kostmann disease) treated with granulocyte colony-stimulating factor-Reference-Cited by-同舟云学术

An abnormal clone with monosomy 7 and trisomy 21 in the bone marrow of a child with congenital agranulocytosis (Kostmann disease) treated with granulocyte colony-stimulating factor

Published:1995-10 Issue:2 Volume:84 Page:99-104
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Shekhter-Levin Sofia,Penchansky Lila,Wollman Michael R.,Sherer Maureen E.,Wald Niel,Gollin Susanne M.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference33 articles.

1. Infantile genetic agranulocytosis;Kostmann;Acta Paediatr Scand,1956

2. Infantile genetic agranulocytosis. A review with presentation of ten new cases;Kostmann;Acta Paediatr Scand,1975

3. Infantile genetic agranulocytosis. Two cases occurring in siblings and one in a distant relative;Rodin;Am J Dis Child,1973

4. Congenital agranulocytosis: prolonged survival and terminal acute leukemia;Gilman;Blood,1970

5. Congenital agranulocytosis terminating in acute myelomonocytic leukemia;Rosen;J Pediatr,1979

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