Chromosome derived from translocation(1;17) retains alphoid sequences of both chromosomes involved.

[1]  F. Patrone,et al.  Trisomy 8 detection in Ph+ CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques. , 1994, Cancer genetics and cytogenetics.

[2]  S. Heim,et al.  Identification of a whole‐arm translocation by in situ hybridization with directly fluorochrome‐labeled probes in a myelodysplastic syndrome , 1992, Genes, chromosomes & cancer.

[3]  B. Vissel,et al.  A SURVEY OF THE GENOMIC DISTRIBUTION OF ALPHA SATELLITE DNA ON ALL THE HUMAN CHROMOSOMES, AND DERIVATION OF A NEW CONSENSUS SEQUENCE , 1991 .

[4]  A. Sandberg The chromosomes in human cancer and leukemia , 1990 .

[5]  H. Willard,et al.  Centromeres of mammalian chromosomes. , 1990, Trends in genetics : TIG.

[6]  H. Willard,et al.  Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[7]  D. Pinkel,et al.  Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[8]  D. Patterson,et al.  Combined trisomy 1q and monosomy 17p due to translocation t(1;17) in a patient with myelodysplastic syndrome. , 1988, Cancer genetics and cytogenetics.

[9]  F. Ajmar,et al.  Correlation between acquired pseudo-Pelger-Huet anomaly and involvement of chromosome 17 in chronic myeloid leukemia. , 1987, Cancer genetics and cytogenetics.

[10]  A. de la Chapelle,et al.  Abnormalities of chromosome No. 17 in myeloproliferative disorders. , 1982, Cancer genetics and cytogenetics.