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Published in Current genomics (05.07.2022)
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Published in Life (Basel, Switzerland) (12.07.2022)
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Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency
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Published in Children (Basel) (10.02.2023)
Published in Children (Basel) (10.02.2023)
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Dental Phenotype with Minor Ectodermal Symptoms Suggestive of IWNT10A/I Deficiency
García-Martínez, Victoria-Eugenia, Galiana-Vallés, Ximo, Zomeño-Alcalá, Otilia, Rodríguez-López, Raquel, Llena, Carmen, Martínez-Romero, María del Carmen, Guillén-Navarro, Encarna
Published in Children (Basel) (01.02.2023)
Published in Children (Basel) (01.02.2023)
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Journal Article
Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency
García-Martínez, Victoria-Eugenia, Galiana-Vallés, Ximo, Zomeño-Alcalá, Otilia, Rodríguez-López, Raquel, Llena, Carmen, Martínez-Romero, María Del Carmen, Guillén-Navarro, Encarna
Published in Children (Basel, Switzerland) (10.02.2023)
Published in Children (Basel, Switzerland) (10.02.2023)
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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
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
Published in Life (Basel, Switzerland) (12.07.2022)
Published in Life (Basel, Switzerland) (12.07.2022)
Get full text
Report