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V P Sybert

Showing results (61-70 of 77) with videos related to

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The Journal of Investigative Dermatology|May 1, 1987
Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormalP Fleckman, K A Holbrook, B A Dale, et al.
The Journal of Investigative Dermatology|April 1, 1983
Epidermolytic hyperkeratosis: ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infantK A Holbrook, B A Dale, V P Sybert, et al.
The Journal of Investigative Dermatology|August 1, 1993
A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosisK Stephens, V P Sybert, E M Wijsman, et al.
The Journal of Investigative Dermatology|March 1, 1997
Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patientsK Stephens, P Ehrlich, M Weaver, et al.
Human Molecular Genetics|December 10, 1999
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesM O Dorschner, V P Sybert, M Weaver, et al.
The New England Journal of Medicine|September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirthsR F Mueller, V P Sybert, J Johnson, et al.
The Journal of Pediatrics|September 1, 1996
Prevalence of hypopigmented macules in a healthy populationS L Vanderhooft, J S Francis, R A Pagon, et al.
Human Genetics|January 1, 1992
Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomesK Stephens, L Kayes, V M Riccardi, et al.
American Journal of Human Genetics|March 1, 1995
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton functionK Stephens, A Zlotogorski, L Smith, et al.
The Journal of Investigative Dermatology|January 1, 1990
Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granulesB A Dale, K A Holbrook, P Fleckman, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
The Journal of Investigative Dermatology|May 1, 1987
Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormalP Fleckman, K A Holbrook, B A Dale, et al.
The Journal of Investigative Dermatology|April 1, 1983
Epidermolytic hyperkeratosis: ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infantK A Holbrook, B A Dale, V P Sybert, et al.
The Journal of Investigative Dermatology|August 1, 1993
A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosisK Stephens, V P Sybert, E M Wijsman, et al.
The Journal of Investigative Dermatology|March 1, 1997
Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patientsK Stephens, P Ehrlich, M Weaver, et al.
Human Molecular Genetics|December 10, 1999
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesM O Dorschner, V P Sybert, M Weaver, et al.
The New England Journal of Medicine|September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirthsR F Mueller, V P Sybert, J Johnson, et al.
The Journal of Pediatrics|September 1, 1996
Prevalence of hypopigmented macules in a healthy populationS L Vanderhooft, J S Francis, R A Pagon, et al.
Human Genetics|January 1, 1992
Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomesK Stephens, L Kayes, V M Riccardi, et al.
American Journal of Human Genetics|March 1, 1995
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton functionK Stephens, A Zlotogorski, L Smith, et al.
The Journal of Investigative Dermatology|January 1, 1990
Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granulesB A Dale, K A Holbrook, P Fleckman, et al.
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