(Q35203957)

7 August 2017

Estimation of male to female ratio of mutation rates from carrier-detection tests in X-linked disorders (English)

1 reference

7 August 2017

Winter RM

1

1 reference

PubMed ID

7395871

7 August 2017

language of work or name

English

0 references

publication date

1 July 1980

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

32

1 reference

7 August 2017

582-588

1 reference

7 August 2017

4

1 reference

Answer to criticism of Morton and Lalouel

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Equilibrium frequencies in X-linked recessive disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Spontaneous frequencies of point mutations in mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Genetic epidemiology of Lesch-Nyhan disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

The laboratory diagnosis of the carrier state for classic hemophilia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Effects of reproductive compensation and genetic drift on X-linked lethals

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Use of overlapping normal distributions in genetic counselling

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Systemic Membrane Defect in the Proximal Muscular Dystrophies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

The sporadic case of haemophilia A.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686120

Spontaneous mutation in man

28 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7395871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Carrier Detection in Duchenne Muscular Dystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7395871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Ascertainment and Age of Onset in Pedigree Analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7395871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1686120

1 reference

7 August 2017

1 reference

PubMed ID

7395871