(Q41685594)

7 October 2017

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts (English)

1 reference

7 October 2017

Sun YJ

1

1 reference

PubMed ID

10449653

7 October 2017

Baumer A

series ordinal

2

1 reference

7 October 2017

1 September 1999

1 reference

American Journal of Medical Genetics Part A

7 October 2017

1 reference

7 October 2017

86

1 reference

7 October 2017

2

1 reference

7 October 2017

162-164

1 reference

Molecular-neurobehavioral associations in females with the fragile X full mutation.

7 October 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Asynchronous DNA synthesis of sex chromatin in human interphase nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Characterization of the full fragile X syndrome mutation in fetal gametes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Molecular heterogeneity of the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

Association of fragile X syndrome with delayed replication of the FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990910%2986%3A2%3C162%3A%3AAID-AJMG14%3E3.0.CO%3B2-D

10.1002/(SICI)1096-8628(19990910)86:2<162::AID-AJMG14>3.0.CO;2-D

21 January 2018

Identifiers

DOI

1 reference

7 October 2017

1 reference

PubMed ID

10449653