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Kenneth Fong

Showing results (11-20 of 26) with videos related to

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The Australasian Journal of Dermatology|August 13, 2011
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10AGabriela Petrof, Kenneth Fong, Joey E Lai-Cheong, et al.
Anais Brasileiros De Dermatologia|September 17, 2015
Is adermatoglyphia an additional feature of Kindler Syndrome?Hiram Larangeira de Almeida, Fernanda Mendes Goetze, Kenneth Fong, et al.
Anais Brasileiros De Dermatologia|December 19, 2013
Sporadic Kindler syndrome with a novel mutationHiram Larangeira de Almeida, Gláucia Thomas Heckler, Kenneth Fong, et al.
Australian Occupational Therapy Journal|August 1, 2018
Factor analysis of the Approaches and Study Skills Inventory for Students in a cross-cultural occupational therapy undergraduate student sampleTore Bonsaksen, Milada C Småstuen, Mikkel M Thørrisen, et al.
Pediatric Dermatology|November 23, 2016
Questioning the Clinical Utility of Exome Sequencing in Developing CountriesKenneth Fong, Celeste V Bailey, Peggy Tuttle, et al.
The Australasian Journal of Dermatology|April 17, 2020
Intravascular large B-cell lymphoma presenting as a nondescript macular eruptionLing Jing Jessica Lee, Kenneth Fong, Sean Leong, et al.
The Journal of Investigative Dermatology|September 13, 2013
BPAG1-e restricts keratinocyte migration through control of adhesion stabilityMagdalene Michael, Rumena Begum, Kenneth Fong, et al.
Pediatric Dermatology|November 10, 2011
Acral peeling skin syndrome: a clinically and genetically heterogeneous disorderSasha Pavlovic, Aleksandar L Krunic, Tanja K Bulj, et al.
Acta Dermato-Venereologica|February 22, 2011
Novel and recurrent FERMT1 gene mutations in Kindler syndromeTanasit Techanukul, Gomathy Sethuraman, Abraham Zlotogorski, et al.
The Journal of Investigative Dermatology|November 25, 2011
Autosomal recessive epidermolysis bullosa simplex due to loss of BPAG1-e expressionLu Liu, Patricia J Dopping-Hepenstal, Patricia A Lovell, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
The Australasian Journal of Dermatology|August 13, 2011
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10AGabriela Petrof, Kenneth Fong, Joey E Lai-Cheong, et al.
Anais Brasileiros De Dermatologia|September 17, 2015
Is adermatoglyphia an additional feature of Kindler Syndrome?Hiram Larangeira de Almeida, Fernanda Mendes Goetze, Kenneth Fong, et al.
Anais Brasileiros De Dermatologia|December 19, 2013
Sporadic Kindler syndrome with a novel mutationHiram Larangeira de Almeida, Gláucia Thomas Heckler, Kenneth Fong, et al.
Australian Occupational Therapy Journal|August 1, 2018
Factor analysis of the Approaches and Study Skills Inventory for Students in a cross-cultural occupational therapy undergraduate student sampleTore Bonsaksen, Milada C Småstuen, Mikkel M Thørrisen, et al.
Pediatric Dermatology|November 23, 2016
Questioning the Clinical Utility of Exome Sequencing in Developing CountriesKenneth Fong, Celeste V Bailey, Peggy Tuttle, et al.
The Australasian Journal of Dermatology|April 17, 2020
Intravascular large B-cell lymphoma presenting as a nondescript macular eruptionLing Jing Jessica Lee, Kenneth Fong, Sean Leong, et al.
The Journal of Investigative Dermatology|September 13, 2013
BPAG1-e restricts keratinocyte migration through control of adhesion stabilityMagdalene Michael, Rumena Begum, Kenneth Fong, et al.
Pediatric Dermatology|November 10, 2011
Acral peeling skin syndrome: a clinically and genetically heterogeneous disorderSasha Pavlovic, Aleksandar L Krunic, Tanja K Bulj, et al.
Acta Dermato-Venereologica|February 22, 2011
Novel and recurrent FERMT1 gene mutations in Kindler syndromeTanasit Techanukul, Gomathy Sethuraman, Abraham Zlotogorski, et al.
The Journal of Investigative Dermatology|November 25, 2011
Autosomal recessive epidermolysis bullosa simplex due to loss of BPAG1-e expressionLu Liu, Patricia J Dopping-Hepenstal, Patricia A Lovell, et al.
Pageof 3