(Q33673700)

28 July 2017

title

Replication status of fragile X(q27.3) in 13 female heterozygotes (English)

1 reference

28 July 2017

Tuckerman E

1

1 reference

28 July 2017

Webb T

series ordinal

2

1 reference

28 July 2017

Thake A

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 October 1986

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

23

1 reference

28 July 2017

issue

5

1 reference

28 July 2017

page(s)

407-410

1 reference

Additional evidence for fragile X activity in heterozygous carriers.

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=1049776

Deleted X chromosomes in patients with the fragile X syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

Four cases of trisomy 18 syndrome with limb reduction malformations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

Activity of the fragile X in heterozygous carriers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

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=1049776

Inactivation pattern of the fragile X in heterozygous carriers.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049776

Replication pattern in XXY cells with fra(X)

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3783617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparison of expression of the fragile site at Xq27 in T and B lymphocytes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3783617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

0 references

1 reference

28 July 2017

1 reference