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chromosomes human, pair 1
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Summary
General Info
Body Atlas
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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Turner Syndrome: Genotype and Phenotype
Phase I Study of Oral BAY 1217389 in Combination With Intravenous Paclitaxel
Evaluation of Patients With Unresolved Chromosome Abnormalities
Genetics of Rheumatoid Arthritis
A Positional Cloning Study on Schizophrenia
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