(Q72666314)

English

Are the mutation rates for the X-chromosomal forms of hemophilia in female gonads lower than in the gonads of males?

scientific article published on 01 January 1965

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Sind die Mutationsraten f�r die X-chromosomal recessiven H�mophilieformen in Keimzellen von Frauen niedriger als in Keimzellen von M�nnern? (German)

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marking inconsistent with the registered/official identifier/name

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

Are the mutation rates for the X-chromosomal forms of hemophilia in female gonads lower than in the gonads of males? (English)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5869749

8 July 2023

1 reference

based on heuristic

inferred from title

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

author name string

F. Vogel

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5869749

8 July 2023

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5869749

8 July 2023

publication date

1 January 1965

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00395656.pdf

Portable Document Format

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

http://link.springer.com/article/10.1007/BF00395656/fulltext.html

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

http://link.springer.com/content/pdf/10.1007/BF00395656

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

253-263

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

THE HEREDITY OF HEMOPHILIA A

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemostatic data in relatives of hemophiliacs A and B; evidence for modifying the classical sex-linked recessive hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemophilia. A study of its laboratory, clinical, genetic and social aspects based on known haemophiliacs in Finland.

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Considerations in Familial Hemorrhagic Disease. I. The Sex-Linked Recessive Disorders, Hemophilia and PTC Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carriers of hemophilia A: a laboratory study

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation rate of the gene for haemophilia, and its segregation ratios in males and females

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary and sporadic genetic trees of hemophiliacs in Switzerland

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SURVEYS ON THE DETERMINATION OF THE MUTATION RATE FOR HEMOPHILIA A AND B IN HAMBURG

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formal genetics of muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Modification of Dahlberg's method for estimation of human mutation rates]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5869749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rate of spontaneous mutation of a human gene

12

1 reference

10.1007/BF00395656

https://api.crossref.org/works/10.1007/BF00395656

8 July 2023

Identifiers

10.1007/BF00395656

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5869749%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

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