Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02529.x/fullpdf
Reference27 articles.
1. Segregation analysis of the X-chromosome in a family with Rett syndrome in two generations;Anvret;Am J Med Genet,1990
2. Rett syndrome: random X chromosome inactivation;Anvret;(Letter to the Editor) Clin Genet,1994
3. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations in the mother of two affected half sisters;Archidiacono;Hum Genet,1991
4. Pattern of replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block;Camargo;Hum Genet,1980
5. Patterns of DNA replication of human chromosomes. II. Replication map and replication model;Camargo;Am J Hum Genet,1982
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1. Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis;Journal of Human Genetics;2007-04-04
2. Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of theFMR2 gene;American Journal of Medical Genetics Part A;2007
3. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X;Annales de Génétique;2004-01
4. Molecular Approaches to the Rett Syndrome Gene;Journal of Child Neurology;1999-12
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