(Q28245138)

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Human genetics. Mapping the way forward

scientific article (publication date: 31 October 1991)

Mapping the way forward

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Human genetics. Mapping the way forward (English)

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Mapping the way forward (English)

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

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K Davies

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publication date

31 October 1991

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

353

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

6347

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

798-9

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798-799

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

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https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Identification of FAP locus genes from chromosome 5q21

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

1 reference

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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Cloning of a gene that is rearranged in patients with choroideraemia

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7 January 2021

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Genetic analysis of autoimmune type 1 diabetes mellitus in mice

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

based on heuristic

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Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

based on heuristic

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Genes for epilepsy mapped in the mouse.

1 reference

https://api.crossref.org/works/10.1038%2F353798A0

7 January 2021

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10.1038/353798A0

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DOI.org query endpoint

https://doi.org/10.1038%2F353798A0

26 March 2017

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