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Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
Bone marrow gene expression of pediatric acute lymphoblastic leukemia
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
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Literature
Most Relevant Literature
DNA double-strand break end synapsis by DNA loop extrusion.
Holding it together: DNA end synapsis during non-homologous end joining.
SYCP1 head-to-head assembly is required for chromosome synapsis in mouse meiosis.
Spontaneous DNA Synapsis by Forming Noncanonical Intermolecular Structures.
Structural maturation of SYCP1-mediated meiotic chromosome synapsis by SYCE3.
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Clinical Trials
Most Relevant Clinical Trials
Growth Hormone and Chromosome 18q- and Abnormal Growth
Variance of HRD From Paired Ovarian Cancer
Prospective Paired Study on the Effectiveness of MitoGrade
Apparently Balanced Chromosomal Translocation/ Next-generation Sequencing/ Intellectual Disability
Evaluation of Patients With Unresolved Chromosome Abnormalities
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