(Q40723842)

English

Antagonistic pleiotropy, mutation accumulation, and human genetic disease

scientific article published on January 1993

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

1 reference

Europe PubMed Central

Antagonistic pleiotropy, mutation accumulation, and human genetic disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

1 reference

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author name string

R L Albin

1

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Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

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publication date

1 January 1993

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Europe PubMed Central

PubMed publication ID

23 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

91

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Europe PubMed Central

PubMed publication ID

23 September 2017

1-3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

279-286

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

https://scigraph.springernature.com/pub.10.1007/bf01436004

0 references

Idiopathic hemochromatosis, an iron storage disease. A. Iron metabolism in hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage between hereditary hemochromatosis and HLA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Huntington disease: genetics and epidemiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative genetics of postponed aging in Drosophila melanogaster. I. Analysis of outbred populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SELECTION FOR DELAYED SENESCENCE IN DROSOPHILA MELANOGASTER.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative genetics of postponed aging in Drosophila melanogaster. II. Analysis of selected lines.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term survival analysis in hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of gene-environment interaction on the expression of longevity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Huntington's chorea. The basis for long-term prevention

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selection for life span in Drosophila melanogaster

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The moulding of senescence by natural selection

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical presentation of hemochromatosis: a changing scene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inheritance of Alzheimer's disease: a new interpretation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8125276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01436004

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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