يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Zomeño-Alcalá, Otilia"', وقت الاستعلام: 0.35s تنقيح النتائج
  1. 1
    Academic Journal
    Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency

    المؤلفون: García-Martínez, Victoria-Eugenia, Galiana-Vallés, Ximo, Zomeño-Alcalá, Otilia, Rodríguez-López, Raquel, Llena Puy, María Carmen, Martínez-Romero, María del Carmen, Guillén-Navarro, Encarna

    المصدر: García-Martínez, Victoria-Eugenia Galiana-Vallés, Ximo Zomeño-Alcalá, Otilia Rodríguez-López, Raquel Llena Puy, María Carmen Martínez-Romero, María del Carmen Guillén-Navarro, Encarna 2023 Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency Children-Basel 10 2 Art. 356

    مصطلحات موضوعية: odontologia

    وصف الملف: application/pdf

    Relation: Children-Basel, 2023, vol. 10, num. 2, p. Art. 356; García-Martínez, V.-E., Galiana-Vallés, X., Zomeño-Alcalá, O., Rodríguez-López, R., Llena, C., Martínez-Romero, M. del C., & Guillén-Navarro, E. (2023). Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency. En Children (Vol. 10, Issue 2, p. 356). MDPI AG. https://doi.org/10.3390/children10020356; https://hdl.handle.net/10550/96647; 164218

    الاتاحة: https://hdl.handle.net/10550/96647
    https://doi.org/10.3390/children10020356

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  2. 2
    Academic Journal
    Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency.

    المؤلفون: García-Martínez, Victoria-Eugenia, Galiana-Vallés, Ximo, Zomeño-Alcalá, Otilia, Rodríguez-López, Raquel, Llena, Carmen, Martínez-Romero, María del Carmen, Guillén-Navarro, Encarna

    المصدر: Children; Feb2023, Vol. 10 Issue 2, p356, 13p

    مصطلحات موضوعية: ECTODERMAL dysplasia, GENETIC mutation, PANORAMIC radiography, SEQUENCE analysis, INCISORS, MOLARS, WNT proteins, HYPODONTIA, GENETIC variation, GENETIC polymorphisms, ALLELES, NAIL diseases, SKIN abnormalities, PHENOTYPES, DISEASE risk factors, SYMPTOMS

    مصطلحات جغرافية: CHINA

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  3. 3
    Academic Journal
    Homozygous Pro1066Arg MYBPC3 Pathogenic Variant in a 26Mb Region of Homozygosity Associated with Severe Hypertrophic Cardiomyopathy in a Patient of an Apparent Non-Consanguineous Family.

    المؤلفون: Rodríguez-López, Raquel, García-Planells, Javier, Martínez-Matilla, Marina, Pérez-García, Cristian, García Banacloy, Amor, Guzmán Luján, Carola, Zomeño Alcalá, Otilia, Belchi Navarro, Joaquina, Martínez-León, Juan, Salguero-Bodes, Rafael

    المصدر: Life (2075-1729); Jul2022, Vol. 12 Issue 7, p1035-1035, 12p

    مصطلحات موضوعية: HYPERTROPHIC cardiomyopathy, HOMOZYGOSITY, HUMAN phenotype, GENETIC variation, GENETIC disorders

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