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Volumn 11, Issue 4, 1998, Pages 875-898
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Childhood myeloproliferative disorders
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Author keywords
Chromosome 7; FISH; JCML; Molecular genetics; Myeloproliferation; Paediatric
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Indexed keywords
APOPTOSIS;
CHROMOSOME 7;
CHROMOSOME DELETION;
CHROMOSOME MAP;
CHRONIC MYELOID LEUKEMIA;
CLINICAL FEATURE;
CYTOGENETICS;
DOWN SYNDROME;
FANCONI ANEMIA;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
HEREDITY;
HUMAN;
MALE;
MOLECULAR GENETICS;
MONOSOMY;
MONOSOMY 7;
MYELODYSPLASTIC SYNDROME;
MYELOPROLIFERATIVE DISORDER;
NEUROFIBROMATOSIS;
NEUTROPENIA;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
REVIEW;
SHWACHMAN SYNDROME;
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EID: 0032323040
PISSN: 09503536
EISSN: None
Source Type: Journal
DOI: 10.1016/S0950-3536(98)80044-9 Document Type: Article |
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Times cited : (2)
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References (167)
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