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Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrow gene expression of pediatric acute lymphoblastic leukemia
Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
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Literature
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Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlati…
An investigation of Ph(1) chromosome in Chronic Myeloid Leukemia patients with different treatment m…
Sequence composition and gene content of the short arm of rye (Secale cereale) chromosome 1.
Fluorescence in situ hybridization identifies complex chromosomal aberrations in multiple myeloma].
Meiotic recombination, synapsis, meiotic inactivation and sperm aneuploidy in a chromosome 1 inversi…
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Lenalidomide in Subject With Low and Intermediate-1 Risk MDS and Without Chromosome 5 Abnormality.
Chromosome 18 Clinical Research Center
The Clinical Study of Sex Chromosome Variants
The eXtroardinarY Babies Study: Natural History of Health and Neurodevelopment in Infants and Young …
Breakpoint Analysis of de Novo Apparently Balanced Chromosomal Translocations
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