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MatchTypeWhy
Genes, DominantConcept Why?
Male-mediated dominant lethal mutations in mice following prooxidant treatment.Academic Article Why?
Smith, FrancisPerson Why?
A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1.Academic Article Why?
APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).Academic Article Why?
Autosomal dominant hypohidrotic ectodermal dysplasia in a large family.Academic Article Why?
Expression of the beta (slow)-isoform of MHC in the adult mouse heart causes dominant-negative functional effects.Academic Article Why?
Familial radioulnar synostosis.Academic Article Why?
Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment.Academic Article Why?
Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencing.Academic Article Why?
A gene for autosomal dominant hypohidrotic ectodermal dysplasia (EDA3) maps to chromosome 2q11-q13.Academic Article Why?
A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.Academic Article Why?
A transgenic mouse model for human autosomal dominant cataract.Academic Article Why?
Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.Academic Article Why?
Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle.Academic Article Why?
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