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Sofia Babay

Showing results (1-10 of 6) with videos related to

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Ophthalmic Genetics|February 20, 2014
Ophthalmologic Findings in H Syndrome: A Unique Diagnostic ClueVered Molho-Pessach, Hadas Mechoulam, Rula Siam, et al.
International Journal of Dermatology|June 6, 2014
IL36RN mutation causing generalized pustular psoriasis in a Palestinian patientYael Renert-Yuval, Liran Horev, Sofia Babay, et al.
Journal of Medical Genetics|March 28, 2014
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hairYuval Ramot, Vered Molho-Pessach, Tomer Meir, et al.
Journal of the American Academy of Dermatology|November 1, 2013
H syndrome: the first 79 patientsVered Molho-Pessach, Yuval Ramot, Frances Camille, et al.
Pediatric Dermatology|April 1, 2015
Two Novel Homozygous Desmoplakin Mutations in Carvajal SyndromeVered Molho-Pessach, Sivan Sheffer, Rula Siam, et al.
Arthritis and Rheumatism|September 29, 2011
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneityYin Liu, Yuval Ramot, Antonio Torrelo, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Ophthalmic Genetics|February 20, 2014
Ophthalmologic Findings in H Syndrome: A Unique Diagnostic ClueVered Molho-Pessach, Hadas Mechoulam, Rula Siam, et al.
International Journal of Dermatology|June 6, 2014
IL36RN mutation causing generalized pustular psoriasis in a Palestinian patientYael Renert-Yuval, Liran Horev, Sofia Babay, et al.
Journal of Medical Genetics|March 28, 2014
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hairYuval Ramot, Vered Molho-Pessach, Tomer Meir, et al.
Journal of the American Academy of Dermatology|November 1, 2013
H syndrome: the first 79 patientsVered Molho-Pessach, Yuval Ramot, Frances Camille, et al.
Pediatric Dermatology|April 1, 2015
Two Novel Homozygous Desmoplakin Mutations in Carvajal SyndromeVered Molho-Pessach, Sivan Sheffer, Rula Siam, et al.
Arthritis and Rheumatism|September 29, 2011
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneityYin Liu, Yuval Ramot, Antonio Torrelo, et al.
Pageof 1