(Q52044359)

English

Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype

scientific article published on May 15, 1992

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scholarly article

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype (English)

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

chromosome fragility

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1605196

14 October 2022

author name string

N. R. Dennis

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1605196

14 October 2022

G. Curtis

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1605196

14 October 2022

J. N. Macpherson

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1605196

14 October 2022

P. A. Jacobs

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1605196

14 October 2022

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1605196

14 October 2022

publication date

1 April 1992

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

15 May 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1605196

14 October 2022

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320430137

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320430137

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

43

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

232-236

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

1-2

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

Genotype prediction in the fragile X syndrome

1

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

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

2

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

Molecular heterogeneity of the fragile X syndrome

4

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

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

5

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

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

6

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation

7

1 reference

10.1002/AJMG.1320430137

https://api.crossref.org/works/10.1002/AJMG.1320430137

14 October 2022

Identifiers

10.1002/AJMG.1320430137

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/1605196

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