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chromosomes human, pair 20
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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
Meningiomas with del(22q), del(1p36), or complex karyotypes associated with del(1p36) or del(14q)
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Ring chromosome 20.
Two siblings with similar phenotypes: one of them had ring 20 chromosome.
Genetic investigations on 8 patients affected by ring 20 chromosome syndrome.
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond sy…
Aneuploid analysis of chromosomes 3, 8, 10, 20 and Y in esophageal squamous cell carcinoma].
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The Association Between Telomere Length and Propofol Dose in Anesthesia-induction
Genetics of Rheumatoid Arthritis
Reduced Intensity Donor Stem Cell Transplant in Treating Patients With High Risk Acute Lymphocytic L…
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
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