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Francisco Cammarata-Scalisi

Showing results (1-10 of 50) with videos related to

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Archivos Argentinos De Pediatria|September 28, 2019
Trisomy 9p. A brief clinical, diagnostic and therapeutic descriptionFrancisco Cammarata-Scalisi
Archivos Argentinos De Pediatria|November 21, 2018
Main genetic entities associated with supernumerary teethFrancisco Cammarata-Scalisi, Andrea Avendaño, Michele Callea
Boletin Medico Del Hospital Infantil De Mexico|March 26, 2019
Cromosoma 13 en anilloFrancisco Cammarata-Scalisi, Yajaira Briceño, Edymar Cegarra, et al.
Hormones (Athens, Greece)|June 3, 2018
5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A reviewAndrea Avendaño, Irene Paradisi, Francisco Cammarata-Scalisi, et al.
Molecular Genetics & Genomic Medicine|May 23, 2019
Clinical and molecular characterization of an 18-month-old infant with autosomal recessive cutis laxa type 1C due to a novel LTBP4 pathogenic variant, and literature reviewMarco Ritelli, Francisco Cammarata-Scalisi, Valeria Cinquina, et al.
Boletin Medico Del Hospital Infantil De Mexico|November 27, 2019
Osteogenesis imperfect: clinical and epidemiological findings in a series of pediatric patientsFrancisco Cammarata-Scalisi, Carlos Ramos-Urrea, Gloria Da Silva
Archivos Argentinos De Pediatria|November 24, 2015
[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]Michele Callea, Izzet Yavuz, Gabriella Clarich, et al.
Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
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 30, 2020
Silver-Russell syndrome. Clinical and etiopathological aspects of a model genomic imprinting entityFrancisco Cammarata-Scalisi, Michele Callea, Frances Stock, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Archivos Argentinos De Pediatria|September 28, 2019
Trisomy 9p. A brief clinical, diagnostic and therapeutic descriptionFrancisco Cammarata-Scalisi
Archivos Argentinos De Pediatria|November 21, 2018
Main genetic entities associated with supernumerary teethFrancisco Cammarata-Scalisi, Andrea Avendaño, Michele Callea
Boletin Medico Del Hospital Infantil De Mexico|March 26, 2019
Cromosoma 13 en anilloFrancisco Cammarata-Scalisi, Yajaira Briceño, Edymar Cegarra, et al.
Hormones (Athens, Greece)|June 3, 2018
5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A reviewAndrea Avendaño, Irene Paradisi, Francisco Cammarata-Scalisi, et al.
Molecular Genetics & Genomic Medicine|May 23, 2019
Clinical and molecular characterization of an 18-month-old infant with autosomal recessive cutis laxa type 1C due to a novel LTBP4 pathogenic variant, and literature reviewMarco Ritelli, Francisco Cammarata-Scalisi, Valeria Cinquina, et al.
Boletin Medico Del Hospital Infantil De Mexico|November 27, 2019
Osteogenesis imperfect: clinical and epidemiological findings in a series of pediatric patientsFrancisco Cammarata-Scalisi, Carlos Ramos-Urrea, Gloria Da Silva
Archivos Argentinos De Pediatria|November 24, 2015
[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]Michele Callea, Izzet Yavuz, Gabriella Clarich, et al.
Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
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 30, 2020
Silver-Russell syndrome. Clinical and etiopathological aspects of a model genomic imprinting entityFrancisco Cammarata-Scalisi, Michele Callea, Frances Stock, et al.
Pageof 5