777 SAM syndrome is characterized by extensive phenotype heterogeneity
Tiaber, S., Mohamad, J., Cohen-Barak, E., Gat, A., Mamlouk, E., Sarig, O., Shalev, S., Sprecher, E.
Published in Journal of investigative dermatology (01.05.2018)
Published in Journal of investigative dermatology (01.05.2018)
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Journal Article
769 Filaggrin 2 deficiency causes generalized peeling of the skin
Mohamad, J., Sarig, O., Peled, A., Malchin, N., Bochner, R., Vodo, D., Rabinowitz, T., Pavlovsky, M., Tiaber, S., Fried, M., Eskin-Schwartz, M., Shomron, N., Uitto, J., Koetsier, J., Godsel, L., Green, K., Bergman, R., Sprecher, E.
Published in Journal of investigative dermatology (01.05.2018)
Published in Journal of investigative dermatology (01.05.2018)
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Journal Article
774 Focal facial dermal dysplasia type I caused by a duplication on 1p36.22
Sarig, O., Hafner, A., Malchin, N., Keydar, I., Fishilevich, S., Isakov, O., Fainberg, G., Samuelov, L., Nousbeck, J., Mohamad, J., Tiaber, S., Rabinowitz, T., Shomron, N., Lancet, D., Ast, G., Sprecher, E.
Published in Journal of investigative dermatology (01.05.2018)
Published in Journal of investigative dermatology (01.05.2018)
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Journal Article
283 Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a middle eastern population
Mohamad, J., Samuelov, L., Malchin, N., Tiaber, S., Rabinowitz, T., Bitterman-Deutsch, O., Molho-Pessach, V., Cohen-Barak, E., Bach, G., Garty, B., Bergman, R., Harel, A., Nanda, A., Lestringant, G., McGrath, J., Shalev, S., Shomron, N., Mashiach, J., Eskin-Schwartz, M., Sarig, O., Sprecher, E.
Published in Journal of investigative dermatology (01.05.2018)
Published in Journal of investigative dermatology (01.05.2018)
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Journal Article