Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome-Reference-Cited by-同舟云学术

Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome

Published:2001-12 Issue: Volume:23 Page:S214-S217
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Yurov Yuri B.,Vorsanova Svetlana G.,Kolotii Alexei D.,Iourov Ivan Y.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference19 articles.

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3. Application of cloned satellite DNA sequences to molecular-cytogenetic analysis of constitutive heterochromatin in man;Yurov;Hum Genet,1987

4. Use of cloned alpha satellite DNA probes for the analysis of polymorphic heterochromatic regions of human chromosomes and parental origin of trisomy 21 (in Russian);Yurov;Genetica,1991

5. High resolution fluorescence in situ hybridization using cyanine and fluorescein dyes: ultra-rapid chromosome detection by directly fluorescently labelled alphoid DNA probes;Yurov;Hum Genet,1996

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1. Svetlana G. Vorsanova (1945–2021);Molecular Cytogenetics;2022-08-19

2. Rett syndrome in Russia and abroad: a scientific historical review;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2020-07-08

3. VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia;Molecular Cytogenetics;2018-12

4. Yuri B. Yurov (1951-2017);Molecular Cytogenetics;2018-06-13

5. Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2015