(Q43143805)

14 November 2017

Genetic epidemiology of Lesch-Nyhan disease (English)

1 reference

14 November 2017

0 references

1 reference

1

Morton NE

1 reference

14 November 2017

2

Lalouel JM

1 reference

14 November 2017

language of work or name

English

0 references

publication date

1 May 1977

1 reference

American Journal of Human Genetics

14 November 2017

1 reference

14 November 2017

29

1 reference

14 November 2017

3

1 reference

14 November 2017

304-311

1 reference

Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

Formal genetics of muscular dystrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

Diagnosis and treatment of the Lesch-Nyhan syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants)

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

The sporadic case of haemophilia A.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685301

Segregation analysis in human genetics

25 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/868879

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Spontaneous mutation in man

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/868879

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/868879

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

14 November 2017

PubMed publication ID

868879

1 reference