(Q34757182)

4 August 2017

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title

Human gene mutation in pathology and evolution (English)

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4 August 2017

1

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4 August 2017

publication date

1 May 2002

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Journal of Inherited Metabolic Disease

4 August 2017

published in

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4 August 2017

volume

25

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4 August 2017

issue

3

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4 August 2017

page(s)

157-182

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https://scigraph.springernature.com/pub.10.1023/a:1015621710660

4 August 2017

exact match

0 references

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Complete nucleotide sequence of the human RCC1 gene involved in coupling between DNA replication and mitosis

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

Molecular genetic analysis of the human Lewis histo-blood group system

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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Cloning of novel trinucleotide-repeat (CAG) containing genes in mouse brain

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12 December 2020

Molecular and population genetic analysis of allelic sequence diversity at the human beta-globin locus

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12 December 2020

Structure and diversity of the T-cell receptor alpha chain in rhesus macaque and chimpanzee.

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12 December 2020

An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels

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12 December 2020

Meiotic microdeletion breakpoints in the BRCA1 gene are significantly associated with symmetric DNA-sequence elements

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12 December 2020

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12 December 2020

Nucleotide substitution at major histocompatibility complex class II loci: evidence for overdominant selection

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Genetics of infectious disease resistance

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12 December 2020

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12 December 2020

Factor V Q506 mutation (activated protein C resistance) associated with reduced intrapartum blood loss--a possible evolutionary selection mechanism

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12 December 2020

Single base-pair substitutions in pathology and evolution: Two sides to the same coin

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https://api.crossref.org/works/10.1023%2FA%3A1015621710660

7 January 2021

Identifiers

DOI

10.1023/A:1015621710660

1 reference

Dimensions Publication ID

4 August 2017

1016544092

0 references

1 reference