about
Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys.Prevalence of deafness and association with coat variations in client-owned ferrets.A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats.A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeysA COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic SyndromeHaplosufficiency of PAX3 for melanoma development in Tyr: NRASQ61K; Cdkn2a-/- mice allows identification and sorting of melanoma cells using a Pax3GFP reporter allele.Clinical characterisation of polydactyly in Maine Coon cats.A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys.Cataracts in a population of Bengal cats in FranceAllelic heterogeneity of albinism in the domestic catGenetic heterogeneity of polydactyly in Maine Coon catsCopal, a new MC1R allele in the domestic catFeline chimerism revealed by DNA profilingDonskoy cats as a new model of oculocutaneous albinism with the identification of a splice-site variant in Hermansky-Pudlak Syndrome 5 gene
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Marie Abitbol
@en
Marie Abitbol
@nl
type
label
Marie Abitbol
@en
Marie Abitbol
@nl
prefLabel
Marie Abitbol
@en
Marie Abitbol
@nl
P108
P31
P496
0000-0002-5615-7897