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chromosomes 17
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OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
Gene expression in neuroblastomas with recurrent genomic alterations
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Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism…
Risk factors for perioperative adverse events in children with myotonic dystrophy.
Karyotypic changes in a multistage model of chemical hepatocarcinogenesis in the rat.
Physical mapping of the K+ transport trkA gene of Escherichia coli and overproduction of the TrkA pr…
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromos…
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Studying Chromosomes in Samples From Younger Patients With Neuroblastoma
Prenatal Molecular Characterisation by CGH+SNP-ARRAY of Supernumerary Marker Chromosomes and de Novo…
FISH in Diagnosis of Biliary Stricture
Study of Tissue and Blood Samples From Patients With Low-Grade Glioma
Genetic Markers in Patients With Colorectal Cancer
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