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Article

Mapping of the flaky skin (fsn) mutation on distal mouse chromosome 17.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Oct 1995

Pelsue S C, Schweitzer P A, Beamer W G, Shultz L D

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Identifiers

PMID: 8563181
DOI: 10.1007/BF00354305

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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Mapping of the flaky skin (fsn) mutation on distal mouse chromosome 17.PMID 8563181Read ↗

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Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.Semantic proximity Read ↗

Thin fur, a recessive mutant on chromosome 17 of the mouse.Semantic proximity Read ↗

A mutant mouse with severe anemia and skin abnormalities controlled by a new allele of the flaky skin (fsn) locus.Semantic proximity Read ↗

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A high-resolution linkage map of the tight skin 2 (Tsk2) locus: a mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases.Semantic proximity Read ↗

Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.Semantic proximity Read ↗

The spontaneous coat color mutant white nose (wn) maps to murine chromosome 15.Semantic proximity Read ↗

The flaky skin (fsn) mutation in mice: map location and description of the anemia.Semantic proximity Read ↗

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Spatially restricted hypopigmentation associated with an Ednrbs-modifying locus on mouse chromosome 10.Semantic proximity Read ↗

Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.Semantic proximity Read ↗

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