Browsing Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 by Author "HADJ-RABIA, Smaïl"
Now showing items 1-3 of 3
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Clinical variability and probable founder effect in oculocutaneous albinism type 7.
BATAILLE, Pauline; MICHAUD, Vincent; ROBERT, Matthieu P ...
(Clinical Genetics. vol. 97, n° 3, pp. 527-528, 2020-03-01)Article de revue -
Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation.
MORENO-ARTERO, Ester; MORICE-PICARD, Fanny; LASSEAUX, Eulalie ...(Genes. vol. 13, n° 12, 2022-11-23)Article de revueOpen access -
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients.
BESSIS, Didier; BURSZTEJN, Anne-Claire; MORICE-PICARD, Fanny ...(Journal of the European Academy of Dermatology and Venereology, 2024-04-10)Article de revueOpen access