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A deletion/insertion polymorphism in the human BCR gene on chromosome 22.Academic Article Why?
Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.Academic Article Why?
Search for a schizophrenia susceptibility locus on human chromosome 22.Academic Article Why?
Chromosomes, Human, Pair 22Concept Why?
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).Academic Article Why?
Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22.Academic Article Why?
A recurring chromosome rearrangement, dic(16;22), in acute nonlymphocytic leukemia.Academic Article Why?
Additional cytogenetic abnormalities in adults with Philadelphia chromosome-positive acute lymphoblastic leukaemia: a study of the Cancer and Leukaemia Group B.Academic Article Why?
DNA methylation profiling of human chromosomes 6, 20 and 22.Academic Article Why?
Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin.Academic Article Why?
Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene.Academic Article Why?
Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.Academic Article Why?
Heterogeneity of genomic fusion of BCR and ABL in Philadelphia chromosome-positive acute lymphoblastic leukemia.Academic Article Why?
Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome.Academic Article Why?
Multicenter linkage study of schizophrenia loci on chromosome 22q.Academic Article Why?
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