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Colin Eric Willoughby

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

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Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
Italian Journal of Pediatrics|August 29, 2020
Membranous aplasia cutis congenita in trisomy 18Francisco Cammarata-Scalisi, Andrea Diociaiuti, Blanca de Guerrero, et al.
Dermatologic Therapy|May 6, 2020
Clinical, etiopathogenic, and therapeutic aspects of KID syndromeFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Antonio Cárdenas Tadich, et al.
Genes|March 25, 2022
Multisystemic Manifestations in Rare Diseases: The Experience of Dyskeratosis CongenitaMichele Callea, Diego Martinelli, Francisco Cammarata-Scalisi, et al.
Ophthalmology|July 2, 2010
Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosaGraeme Richard Clark, Paul Crowe, Dorota Muszynska, et al.
Investigacion Clinica|June 26, 2018
A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotypeMichele Callea, Colin Eric Willoughby, Francisco Camarata-Scalisi, et al.
Genes|March 25, 2022
Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to ManagementFrancisco Cammarata-Scalisi, Michele Callea, Diego Martinelli, et al.
Pageof 1

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

Sort By:
Pageof 1
Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
Italian Journal of Pediatrics|August 29, 2020
Membranous aplasia cutis congenita in trisomy 18Francisco Cammarata-Scalisi, Andrea Diociaiuti, Blanca de Guerrero, et al.
Dermatologic Therapy|May 6, 2020
Clinical, etiopathogenic, and therapeutic aspects of KID syndromeFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Antonio Cárdenas Tadich, et al.
Genes|March 25, 2022
Multisystemic Manifestations in Rare Diseases: The Experience of Dyskeratosis CongenitaMichele Callea, Diego Martinelli, Francisco Cammarata-Scalisi, et al.
Ophthalmology|July 2, 2010
Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosaGraeme Richard Clark, Paul Crowe, Dorota Muszynska, et al.
Investigacion Clinica|June 26, 2018
A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotypeMichele Callea, Colin Eric Willoughby, Francisco Camarata-Scalisi, et al.
Genes|March 25, 2022
Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to ManagementFrancisco Cammarata-Scalisi, Michele Callea, Diego Martinelli, et al.
Pageof 1