Literature DB >> 2696961

Centromere separation and aneuploidy in human mitotic mutants: Roberts syndrome.

E W Jabs1, C M Tuck-Muller, R Cusano, J B Rattner.   

Abstract

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Mesh：

Year:  1989        PMID： 2696961

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN： 0361-7742


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  4 in total

Review 1.  Review and hypothesis: Alzheimer disease and Down syndrome--chromosome 21 nondisjunction may underlie both disorders.

Authors:  H Potter
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism.

Authors:  E W Jabs; C M Tuck-Muller; R Cusano; J B Rattner
Journal:  Chromosoma       Date:  1991-05       Impact factor: 4.316

3.  Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion.

Authors:  Fajian Hou; Hui Zou
Journal:  Mol Biol Cell       Date:  2005-06-15       Impact factor: 4.138

4.  Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells.

Authors:  Lisa D McDaniel; Darrell J Tomkins; Eric J Stanbridge; Martin J Somerville; Errol C Friedberg; Roger A Schultz
Journal:  Am J Hum Genet       Date:  2005-05-10       Impact factor: 11.025
  4 in total

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