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McGrath, John

One or more keywords matched the following items that are connected to McGrath, John

Item Type	Name
Concept	Genes, Dominant
Academic Article	Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.
Academic Article	Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.
Academic Article	Human hair abnormalities resulting from inherited desmosome gene mutations.
Academic Article	Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.
Academic Article	Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR.
Academic Article	A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease.
Academic Article	Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait.
Academic Article	Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.
Academic Article	Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic?Ichthyosis.

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Genes Dominant

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