(Q36756225)

English

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

scientific article published on November 1993

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

author name string

T Arinami

1

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

M Asano

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

K Kobayashi

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

H Yanagi

4

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

H Hamaguchi

5

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

publication date

1 November 1993

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

92

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

431-436

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of founder chromosomes in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of average heterozygosity and genetic distance from a small number of individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and expression of a cDNA encoding the human androgen receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of the fragile X syndrome in Japanese mentally retarded males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA typing and genetic mapping with trimeric and tetrameric tandem repeats

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Description and validation of a method for simultaneous estimation of effective population size and mutation rate from human population data

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8244331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00216445

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

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