Chromosomes, Human, Pair 17 Concept

subject area of

• Chromosomal damage induced by human adenovirus type 12 requires expression of the E1B 55-kilodalton viral protein  Journal Articles
• Chromosome 17 centromere (CEP17) duplication as a predictor of anthracycline response: evidence from the NCIC Clinical Trials Group (NCIC CTG) MA.5 Trial  Journal Articles
• Chromosome-specific subsets of human alpha satellite DNA: Analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat  Journal Articles
• Clinical and molecular delineation of the 17q21.31 microdeletion syndrome  Journal Articles
• Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12  Journal Articles
• Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17  Journal Articles
• Generation of a new adenovirus type 12-inducible fragile site by insertion of an artificial U2 locus in the human genome.  Journal Articles
• Linkage analysis of 26 Canadian breast and breast-ovarian cancer families  Journal Articles
• Macrocephaly, growth failure, translucent skin, renal cysts, coarctation of the aorta, and cholestasis: novel features of a new syndrome – the del17q12 syndrome  Journal Articles
• Microdeletion in distal 17p13.1: A recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability  Journal Articles
• Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation  Journal Articles
• Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: Implications for linkage in neurofibromatosis  Journal Articles
• Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin.  Journal Articles
• PML/RARα APL with undifferentiated morphology and stem cell immunophenotype  Journal Articles
• Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene  Journal Articles
• Renal cell carcinoma with mixed features of papillary and clear cell cytomorphology: a fluorescent in situ hybridization study  Journal Articles
• Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome.  Journal Articles
• The Transcriptionally Competent U2 Gene Is Necessary and Sufficient for Adenovirus Type 12 Induction of the Fragile Site at 17q21-22  Journal Articles
• The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes  Journal Articles