(Q44819900)

English

Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families

scientific article published in October 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Duchenne muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

C R Müller

1

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

T Grimm

2

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

publication date

1 October 1986

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

74

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

181-183

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation rate in Duchenne type of muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection and genetic counselling in duchenne muscular dystrophy (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in human populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous mutation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The estimation of recurrence risks in monogenic disorders using flanking marker loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No sex difference in mutations rates of Duchenne muscular dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier Detection in Duchenne Muscular Dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. A population study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic Membrane Defect in the Proximal Muscular Dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum creatine kinase and sulphydryl concentration after ischemic forearm work in patients and carriers of Duchenne's progressive muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of new mutants among boys with Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. Frequency of sporadic cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3464560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282088

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

release_itimycu2krgera6s5z3dt6q5ae

1 reference

https://api.fatcat.wiki/v0/release/itimycu2krgera6s5z3dt6q5ae

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

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