Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

Author:

Callen D F,Ringenbergs M L,Fowler J C,Freemantle C J,Haan E A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15;Schreck, R.R.; Breg, W.R.; Erlanger, B.F.; Miller, O.J.;Hum Genet,1977

2. Cytogenetic and clinical studies in five cases of inv dup(15);Wisniewski, L.; Hassold, T.; Heffelfinger, J.; Higgins, J.V.;Hum Genet,1979

3. Hierarchical order in chromosome-specific human alpha satellite DNA;Willard, H.F.; Waye, J.S.;Trends Genet,1987

4. Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis;Moyzis, R.K.; Albright, K.L.; Bartholdi, M.F.;Chromosoma,1987

5. Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequences;Jabs, E.W.; Persico, M.G.;Am J Hum Genet,1987

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