(Q33671874)

28 July 2017

title

Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence (English)

1 reference

28 July 2017

Tuckerman E

1

1 reference

28 July 2017

Webb T

series ordinal

2

1 reference

28 July 2017

Bundey SE

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1985

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

22

1 reference

28 July 2017

issue

2

1 reference

28 July 2017

page(s)

85-91

1 reference

Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

Four cases of trisomy 18 syndrome with limb reduction malformations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

Activity of the fragile X in heterozygous carriers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

14 July 2018

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

X-chromosome inactivation and developmental patterns in mammals

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

X-linked mental retardation: a study of 7 families.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

The marker (X) syndrome: a cytogenetic and genetic analysis.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049390

Apparent homozygosity for the fragile site at Xq28 in a normal female

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4039370

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Replication pattern in XXY cells with fra(X)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4039370

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1049390

1 reference

28 July 2017

1 reference