Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype

Cytogenetic and Genome Research

Volumn 129, Issue 4, 2010, Pages 275-279

  Rao, P N ^a   Li, W ^a   Vissers, L E L M ^b   Veltman, J A ^b   Ophoff, R A ^a,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

17q21.31 microdeletion; Genomic disorder; H1 and H2 haplotypes; Inversion polymorphism; Recurrent

Indexed keywords

TAU PROTEIN; TAU PROTEIN H1; TAU PROTEIN H2; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 17Q; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME STRUCTURE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HAPLOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; MICRODELETION SYNDROME; PRIORITY JOURNAL;

ALLELES; CELL LINE; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOMES, HUMAN, PAIR 17; GENETIC LOCI; HAPLOTYPES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; TAU PROTEINS;

HOMO;

EID: 77955717301     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000315901     Document Type: Article

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