Formal genetics of muscular dystrophy (Q35911789)

11 August 2017

Formal genetics of muscular dystrophy (English)

1 reference

11 August 2017

MORTON NE

1

1 reference

11 August 2017

CHUNG CS

series ordinal

2

1 reference

11 August 2017

N. E. MORTON

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

1 March 2024

C. S. CHUNG

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

1 March 2024

language of work or name

English

0 references

publication date

1 December 1959

1 reference

full work available at URL

11 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/14424475/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/14424475/pdf/?tool=EBI

1 March 2024

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

https://europepmc.org/articles/PMC1932041

1 March 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

https://europepmc.org/articles/PMC1932041?pdf=render

1 March 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14424475

American Journal of Human Genetics

1 March 2024

published in

1 reference

11 August 2017

11

1 reference

11 August 2017

360-379

1 reference

The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations.

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Discrimination of genetic entities in muscular 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=1932041

Genetic tests under incomplete ascertainment

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Muscular dystrophy in Northern Ireland. IV. Some additional data

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Some possibilities for measuring selection intensities 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=1932041

The use of the fertilities of affected individuals and their unaffected sibs in the estimation of fitness

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

A genetic study of multiple polyposis of the colon with an appendix deriving a method of estimating relative fitness

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Parental age and mutation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

Heredity counselling for sex-linked recessive deficiency diseases

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1932041

A Presumptive Human XXY/XX Mosaic

24 September 2018

1 reference

12 December 2020

STUDIES IN DISORDERS OF MUSCLE. II. CLINICAL MANIFESTATIONS AND INHERITANCE OF FACIOSCAPULOHUMERAL DYSTROPHY IN A LARGE FAMILY

1 reference

12 December 2020

Colour blindness and the Duchenne-type muscular dystrophy

1 reference

12 December 2020

Segregation analysis in human genetics

1 reference

12 December 2020

On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies

1 reference

12 December 2020

Estimates of the sex ratio of mutation rates in sex-linked conditions by the method of maximum likelihood

1 reference

12 December 2020

The sex ratio of mutation rates of sex-linked recessive genes in man with particular reference to Duchenne type muscular dystrophy

1 reference

12 December 2020

Mutation in the sex-linked recessive type of muscular dystrophy; a possible sex difference

1 reference

12 December 2020

Muscular dystrophy in Northern Ireland. II. An account of nine additional families

1 reference

12 December 2020

Identifiers

1 reference

11 August 2017

1 reference