(Q68231420)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

title

A reinvestigation of thirty three fragile(X) families using probe StB12.3 (English)

1 reference

Crossref

https://api.crossref.org/works/10.1002/AJMG.1320430535

20 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1642285

20 October 2022

Macpherson J

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Harvey J

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Curtis G

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Webb T

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Heitz D

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Rousseau F

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Jacobs P

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1642285

20 October 2022

publication date

1 July 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

15 July 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1642285

full work available at URL

20 October 2022

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320430535

1 reference

Crossref

https://api.crossref.org/works/10.1002/AJMG.1320430535

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320430535

20 October 2022

1 reference

Crossref

https://api.crossref.org/works/10.1002/AJMG.1320430535

American Journal of Medical Genetics Part A

20 October 2022

language of work

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

volume

1 reference

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22 September 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

page(s)

905-912

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

22 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

Molecular heterogeneity of the fragile X syndrome

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

20 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320430535

20 October 2022

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1642285%20AND%20SRC:MED&resulttype=core&format=json