Manière, Marie-Cécile
Hôpitaux Universitaires de Strasbourg
3 papers on CoChat
Most cited papers
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Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases
Cluzeau, C., Hadj-Rabia, S., Jambou, M., Mansour, S., Guigue, P., Masmoudi, S., Bal, E., Chassaing, N., Vincent, M.-C., Viot, G., et al. (2011) · Human Mutation
dental development and anomaliesGenetic and rare skin diseases.
Cited by 311
- Verified
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti
Bodemer, C., Diociaiuti, A., Hadj‐Rabia, S., Robert, M. P., Desguerre, I., Manière, M. ‐., de la Dure‐Molla, M., De Liso, P., Federici, M., Galeotti, A., et al. (2020) · Journal of the European Academy of Dermatology and Venereology
Genetic and rare skin diseases.Dermatology and Skin Diseases
Cited by 59
- Verified
Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study
Friedlander, L., Berdal, A., Boizeau, P., Licht, B. A., Manière, M.-C., Picard, A., Azzis, O., Vazquez, M.-P., Alberti, C., & Molla, M. D. L. D. (2019) · Orphanet Journal of Rare Diseases
Dental Health and Care Utilizationdental development and anomalies
Cited by 30
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