(Q38945173)

7 September 2017

Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population (English)

1 reference

7 September 2017

1 reference

Chiurazzi P

1

1 reference

7 September 2017

Destro-Bisol G

2

1 reference

7 September 2017

Genuardi M

3

1 reference

7 September 2017

Oostra BA

4

1 reference

7 September 2017

Spedini G

5

1 reference

7 September 2017

Neri G

6

1 reference

7 September 2017

1 July 1996

1 reference

American Journal of Medical Genetics Part A

7 September 2017

1 reference

7 September 2017

64

1 reference

7 September 2017

1

1 reference

7 September 2017

216-219

1 reference

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

7 September 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

High resolution of human evolutionary trees with polymorphic microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Mutational processes of simple-sequence repeat loci in human populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

The Y chromosome and the origin of all of us (men)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Population genetics of trinucleotide repeat polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Conservation of CGG region in FMR1 gene in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Trinucleotide diseases on the rise

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Evidence of founder chromosomes in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Haplotype analysis at the FRAXA locus in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Microsatellite evolution--evidence for directionality and variation in rate between species

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

Prevalence of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C216%3A%3AAID-AJMG39%3E3.0.CO%3B2-O

10.1002/(SICI)1096-8628(19960712)64:1<216::AID-AJMG39>3.0.CO;2-O

21 January 2018

Identifiers

DOI

1 reference

7 September 2017

1 reference