(Q33670747)

28 July 2017

title

Fragile X trait in a large kindred: transmission also through normal males (English)

1 reference

28 July 2017

Van Roy BC

1

1 reference

28 July 2017

De Smedt MC

2

1 reference

28 July 2017

Raes RA

3

1 reference

28 July 2017

Dumon JE

4

1 reference

28 July 2017

Leroy JG

5

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 1983

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

20

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

286-289

1 reference

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

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=1049121

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

Fragile X-linked mental retardation: the Martin-Bell syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

Marker X syndrome in an oriental family with probable transmission by a normal male

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049121

Fragile X in a normal male: a cautionary tale

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6620329

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Transmission of fragile (X) (q27) site from a male

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6620329

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Transmission of fragile (X)(q27) from normal male(s)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6620329

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1049121

1 reference

28 July 2017

1 reference