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chromosomes human, pair 14
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Body Atlas
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Most Correlated Studies
OMIM - Congenital chromosomal disease
Bone marrows from acute myleoid leukemia (AML) patients grouped by chromosomal abnormalities
Meningiomas with del(22q), del(1p36), or complex karyotypes associated with del(1p36) or del(14q)
Molecular signature of the t(12;14) subgroup of uterine leiomyomata
T-cell prolymphocytic leukemia (TPLL) and normal T cells
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Literature
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Epilepsy in ring 14 chromosome syndrome.
Ring 14 chromosome presenting as early-onset isolated partial epilepsy.
Molecular cytogenetic characterization of a non-robertsonian dicentric chromosome 14;19 identified i…
Array CGH defined interstitial deletion on chromosome 14: a new case.
Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14.
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Most Relevant Clinical Trials
A Positional Cloning Study on Schizophrenia
Molecular Genetic Study of Schizophrenia: Parent-Offspring Trios
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
Molecular Epidemiology of Childhood Leukemia (Aka The California Childhood Leukemia Study)
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