BIOMEDICINA DE ENFERMEDADES RARAS
French Institute of Health and Medical Research
París, FranciaPublicaciones en colaboración con investigadores/as de French Institute of Health and Medical Research (1)
2017
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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia
Clinical Genetics, Vol. 92, Núm. 1, pp. 91-98