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Fanny Morice-Picard

Showing results (11-20 of 105) with videos related to

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Pediatric Dermatology|February 22, 2019
Isolated straight hair nevus in a White childLucie Rault, Fanny Morice-Picard, Isabelle Svahn, et al.
Social Science & Medicine (1982)|January 30, 2025
Dyadic adjustment of persons with albinism and their significant other: A Bayesian mediation model of the Actor-Partner Interdependence (APIMeM)Hugo Fournier, Nicolas Pillaud, Fanny Morice-Picard, et al.
The British Journal of Dermatology|January 10, 2022
SCN10A variants associated with congenital harlequin syndromeAurelie Halle, Alix De Becdelievre, Benoit Funalot, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
New clinico-genetic classification of trichothiodystrophyFanny Morice-Picard, Muriel Cario-André, Hamid Rezvani, et al.
Pigment Cell & Melanoma Research|September 30, 2008
Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspectsCaroline Rooryck, Fanny Morice-Picard, Nursel H Elçioglu, et al.
Pigment Cell & Melanoma Research|November 6, 2008
Segmental vitiligo as the possible expression of cutaneous somatic mosaicism: implications for common non-segmental vitiligoAlain Taïeb, Fanny Morice-Picard, Thomas Jouary, et al.
Orphanet Journal of Rare Diseases|September 20, 2018
Burden of albinism: development and validation of a burden assessment toolFanny Morice-Picard, Charles Taïeb, Aurelie Marti, et al.
Clinical and Experimental Dermatology|August 7, 2024
Hypohidrotic ectodermal dysplasia in a family: expanding spectrum of LEF1-related disordersAli Hassan, Fanny Morice-Picard, Victor Marin, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropeniaAkio Tanaka, Fanny Morice-Picard, Didier Lacombe, et al.
Clinical and Experimental Dermatology|May 4, 2023
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosisFanny Morice-Picard, Pierre-Louis Lanvin, Eulalie Lasseaux, et al.
Pageof 11

Showing results (11-20 of 105) with videos related to

Sort By:
Pageof 11
Pediatric Dermatology|February 22, 2019
Isolated straight hair nevus in a White childLucie Rault, Fanny Morice-Picard, Isabelle Svahn, et al.
Social Science & Medicine (1982)|January 30, 2025
Dyadic adjustment of persons with albinism and their significant other: A Bayesian mediation model of the Actor-Partner Interdependence (APIMeM)Hugo Fournier, Nicolas Pillaud, Fanny Morice-Picard, et al.
The British Journal of Dermatology|January 10, 2022
SCN10A variants associated with congenital harlequin syndromeAurelie Halle, Alix De Becdelievre, Benoit Funalot, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
New clinico-genetic classification of trichothiodystrophyFanny Morice-Picard, Muriel Cario-André, Hamid Rezvani, et al.
Pigment Cell & Melanoma Research|September 30, 2008
Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspectsCaroline Rooryck, Fanny Morice-Picard, Nursel H Elçioglu, et al.
Pigment Cell & Melanoma Research|November 6, 2008
Segmental vitiligo as the possible expression of cutaneous somatic mosaicism: implications for common non-segmental vitiligoAlain Taïeb, Fanny Morice-Picard, Thomas Jouary, et al.
Orphanet Journal of Rare Diseases|September 20, 2018
Burden of albinism: development and validation of a burden assessment toolFanny Morice-Picard, Charles Taïeb, Aurelie Marti, et al.
Clinical and Experimental Dermatology|August 7, 2024
Hypohidrotic ectodermal dysplasia in a family: expanding spectrum of LEF1-related disordersAli Hassan, Fanny Morice-Picard, Victor Marin, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropeniaAkio Tanaka, Fanny Morice-Picard, Didier Lacombe, et al.
Clinical and Experimental Dermatology|May 4, 2023
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosisFanny Morice-Picard, Pierre-Louis Lanvin, Eulalie Lasseaux, et al.
Pageof 11