Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere

Author:

Warburton Peter E.,Dolled Marisa,Mahmood Radma,Alonso Alicia,Li Shulan,Naritomi Kenji,Tohma Takaya,Nagai Toshiro,Hasegawa Tomonobu,Ohashi Hirofumi,Govaerts Lutgarde C.P.,Eussen Bert H.J.,Van Hemel Jan O.,Lozzio Carmen,Schwartz Stuart,Dowhanick-Morrissette Jennifer J.,Spinner Nancy B.,Rivera Horacio,Crolla John A.,Yu Chih-yu,Warburton Dorothy

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference55 articles.

1. Mitotic phosphorylation of SUV39H1, a novel component of active centromeres, coincides with transient accumulation at mammalian centromeres;Aagaard;J Cell Sci,2000

2. dup(10q) lacking α-satellite DNA in bone marrow cells of a patient with acute myeloid leukemia;Abeliovich;Cancer Genet Cytogenet,1996

3. Alonso A, Li S, Warburton PE. Analysis of the structure and function of the human centromere/kinetochore complex using combined immunofluorescence and FISH to normal and variant centromeres. In: Speel E-JM, Hopman AHN (eds) Chromosome analysis protocols. Humana Press, Totowa, NJ (in press)

4. Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype;Barbi;Am J Med Genet,2000

5. Sequence analysis of an 80 kb human neocentromere DNA;Barry;Hum Mol Genet,1999

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