(Q35743415)

10 August 2017

title

FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability (English)

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10 August 2017

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2

N E Morton

1 reference

10 August 2017

J W Teague

1

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10 August 2017

N R Dennis

3

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10 August 2017

G Curtis

4

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10 August 2017

N McKechnie

5

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10 August 2017

J N Macpherson

6

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10 August 2017

A Murray

7

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10 August 2017

M C Pound

8

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10 August 2017

A J Sharrock

9

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10 August 2017

S A Youings

10

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10 August 2017

P A Jacobs

11

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10 August 2017

language of work or name

English

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publication date

1 January 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

10 August 2017

published in

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10 August 2017

volume

95

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10 August 2017

issue

2

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10 August 2017

page(s)

719-724

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Genetic tests under incomplete ascertainment

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Segregation distortion of the CTG repeats at the myotonic dystrophy locus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Cheaters sometimes prosper: distortion of mendelian segregation by meiotic drive

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Non-Mendelian transmission in a human developmental disorder: split hand/split foot

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Meiotic drive at the myotonic dystrophy locus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Meiotic drive and myotonic dystrophy.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Incidence and mutation rates of structural rearrangements of the autosomes in man.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

27 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

Human female meiosis: new insights into an error-prone process

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18487

Meiotic drive at the myotonic dystrophy locus?

25 September 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

The effect of structural aberrations of the chromosomes on reproductive fitness in man

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

Segregation of delta F508 and normal CFTR alleles in human sperm

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.2.719

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/9435259

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.2.719

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10 August 2017

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10 August 2017

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