CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations

Por Basel-Vanagaite, L., Pasmanik-Chor, M., Lurie, R., Yeheskel, A., Kjaer, K.W.
Publicado em 2011

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity

Por Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M
Publicado em 2003

A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia

Por Solomon-Zemler, R, Basel-Vanagaite, L, Steier, D, Yakar, S, Mel, E, Phillip, M, Bazak, L, Bercovich, D, Werner, H, de Vries, L
Publicado no Endocr Connect (2017)

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation

Por Basel‐Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M
Publicado em 2006