(Q70913450)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

0 references

P Camus

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

N Abbadi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

M C Perrier

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

M Chéry

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

S Gilgenkrantz

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

publication date

1 February 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

volume

97

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

page(s)

247-250

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf02265275

14 October 2019

exact match

0 references

cites work

Expression of the gene defect in X-linked agammaglobulinemia

1 reference

12 December 2020

Tissue specificity of X-chromosome inactivation patterns

1 reference

12 December 2020

A de novo X;3 translocation in Rett syndrome

1 reference

12 December 2020

A newly defined X-linked trait in man with demonstration of the Lyon effect in carrier females

1 reference

12 December 2020

X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease

1 reference

12 December 2020

Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency

1 reference

12 December 2020

Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome

1 reference

12 December 2020

Prevalence study of Rett syndrome in North Dakota children

1 reference

12 December 2020

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

12 December 2020

Metabolic interference and the + - heterozygote. a hypothetical form of simple inheritance which is neither dominant nor recessive

1 reference

12 December 2020

Carrier detection in the Wiskott Aldrich syndrome

1 reference

12 December 2020

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

1 reference

12 December 2020

The Rett Syndrome: the recent advances in genetic studies in the USA

1 reference

12 December 2020

Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

12 December 2020

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

12 December 2020

Another model for the inheritance of Rett syndrome

1 reference

12 December 2020

Rett syndrome: random X chromosome inactivation

1 reference

12 December 2020

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

1 reference

12 December 2020

The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome.

1 reference

12 December 2020

X inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27 beta probe

1 reference

12 December 2020

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

1 reference

12 December 2020

Rett syndrome: genetic clues based on mitochondrial changes in muscle.

1 reference

12 December 2020

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

12 December 2020

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

12 December 2020

Parental origin of the X chromosomes in Rett syndrome

1 reference

12 December 2020

Tokyo symposium on the Rett syndrome: neurobiological approach--concluding remarks and epilogue

1 reference

12 December 2020

A rapid method for the purification of DNA from blood

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02265275

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566963%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference