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QuickView for chromosomes human, pair 22
Most Correlated Studies
- OMIM - Congenital chromosomal disease
- OMIM - Congenital disorder
- Bone marrow gene expression of pediatric acute lymphoblastic leukemia
- 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)
Most Relevant Literature
- Genetics of kidney disorders in Phelan-McDermid syndrome: evidence from 357 registry participants.
- Depression and Catatonia Associated With Lansoprazole in an Adolescent With Phelan-McDermid Syndrome…
- A complex t(15;22;17)(q22;q11.2;q21) variant of APL.
- Clinical and molecular cytogenetic findings of cat eye syndrome and a 2-year-old patient with congen…
- Consensus recommendations on lymphedema in Phelan-McDermid syndrome.
Most Relevant Clinical Trials
- A Positional Cloning Study on Schizophrenia
- Molecular Genetic Study of Schizophrenia: Parent-Offspring Trios
- 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
