(Q34460594)

2 August 2017

A new assay for the analysis of X-chromosome inactivation in carriers with an X-linked disease (English)

1 reference

2 August 2017

Kubota T

1

1 reference

2 August 2017

1 December 2001

1 reference

2 August 2017

Brain and Development

1 reference

2 August 2017

23 Suppl 1

1 reference

2 August 2017

S177-81

1 reference

Gene action in the X-chromosome of the mouse (Mus musculus L.)

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

New Giemsa method for the differential staining of sister chromatids

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Methylation analysis of the fragile X syndrome by PCR.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Mutation screening in Rett syndrome patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900361-8

7 January 2021

10.1016/S0387-7604(01)00361-8

Identifiers

DOI

1 reference

release_nqafpwvkenge5isxsersf66wey

2 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nqafpwvkenge5isxsersf66wey

24 November 2022

mapped directly with Wikidata item

PubMed ID

11738868

1 reference

PubMed ID

11738868