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Dianora Araque

Showing results (1-10 of 7) with videos related to

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Boletin Medico Del Hospital Infantil De Mexico|September 20, 2019
Trisomy 13 mosaicismFrancisco Cammarata-Scalisi, Dianora Araque, Rosmary Ramírez, et al.
Archivos Argentinos De Pediatria|May 8, 2019
[Clinical, biochemical and molecular findings of propionic acidemia]Francisco Cammarata-Scalisi, Chiu Yen-Hui, Liu Tze-Tze, et al.
Molecular Syndromology|June 14, 2019
A Venezuelan Case of Schmid-Type Metaphyseal Chondrodysplasia with a Novel Mutation in <i>COL10A1</i>Francisco Cammarata-Scalisi, Uta Matysiak, Tanja Velten, et al.
Acta Gastroenterologica Latinoamericana|September 11, 2015
[Gastrointestinal obstruction in the mosaic trisomy X]Francisco Cammarata-Scalisi, Dianora Araque, Frances Stock, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Archivos Argentinos De Pediatria|July 25, 2019
[Wolf-Hirschhorn syndrome. Description of five cases characterized by means of single nucleotide polymorphism microarrays]Francisco Cammarata-Scalisi, Raquel Blanco Lago, Pilar Barruz Galián, et al.
Archivos Argentinos De Pediatria|May 16, 2017
[Mosaic trisomy 18. Series of cases]Francisco Cammarata-Scalisi, María A Lacruz-Rengel, Dianora Araque, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Boletin Medico Del Hospital Infantil De Mexico|September 20, 2019
Trisomy 13 mosaicismFrancisco Cammarata-Scalisi, Dianora Araque, Rosmary Ramírez, et al.
Archivos Argentinos De Pediatria|May 8, 2019
[Clinical, biochemical and molecular findings of propionic acidemia]Francisco Cammarata-Scalisi, Chiu Yen-Hui, Liu Tze-Tze, et al.
Molecular Syndromology|June 14, 2019
A Venezuelan Case of Schmid-Type Metaphyseal Chondrodysplasia with a Novel Mutation in <i>COL10A1</i>Francisco Cammarata-Scalisi, Uta Matysiak, Tanja Velten, et al.
Acta Gastroenterologica Latinoamericana|September 11, 2015
[Gastrointestinal obstruction in the mosaic trisomy X]Francisco Cammarata-Scalisi, Dianora Araque, Frances Stock, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Archivos Argentinos De Pediatria|July 25, 2019
[Wolf-Hirschhorn syndrome. Description of five cases characterized by means of single nucleotide polymorphism microarrays]Francisco Cammarata-Scalisi, Raquel Blanco Lago, Pilar Barruz Galián, et al.
Archivos Argentinos De Pediatria|May 16, 2017
[Mosaic trisomy 18. Series of cases]Francisco Cammarata-Scalisi, María A Lacruz-Rengel, Dianora Araque, et al.
Pageof 1