Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

Blood

Volumn 99, Issue 12, 2002, Pages 4638-4641

  Boultwood, Jacqueline ^a,b,c,d   Fidler, Carrie ^a,b,c,d   Strickson, Amanda J ^a,b,c,d   Watkins, Fiona ^a,b,c,d   Gama, Susana ^a,b,c,d   Kearney, Lyndal ^a,b,c,d   Tosi, Sabrina ^a,b,c,d   Kasprzyk, Arek ^a,b,c,d   Cheng, Jan Fang ^a,b,c,d   Jaju, Rina J ^a,b,c,d   Wainscoat, James S ^a,b,c,d  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^d LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 5Q; CLINICAL ARTICLE; DNA POLYMORPHISM; EXPRESSED SEQUENCE TAG; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE SEQUENCE; GENOME; HEMATOPOIETIC STEM CELL; HUMAN; HUMAN CELL; KARYOTYPE; MYELODYSPLASTIC SYNDROME; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STEM CELL;

EID: 0037097597     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V99.12.4638     Document Type: Article

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