Toward understanding the genetic basis of neural tube defectsKIBAR, Z; CAPRA, V; GROS, P et al.Clinical genetics. 2007, Vol 71, Num 4, pp 295-310, issn 0009-9163, 16 p.Article

Contribution of VANGL2 mutations to isolated neural tube defectsKIBAR, Z; SALEM, S; BOSOI, C. M et al.Clinical genetics. 2011, Vol 80, Num 1, pp 76-82, issn 0009-9163, 7 p.Article

Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French familyLAMARTINE, J; LAOUDJ, D; BLANCHET-BARDON, C et al.British journal of dermatology (1951). 2000, Vol 142, Num 2, pp 248-252, issn 0007-0963Article

A radiation hybrid map of 48 loci including the Clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13qKIBAR, Z; LAFRENIERE, R. G; CHAKRAVARTI, A et al.Genomics (San Diego, Calif.). 1999, Vol 56, Num 1, pp 127-130, issn 0888-7543Article

Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3LAFRENIERE, R. G; ROCHEFORT, D. L; ROMMENS, J. M et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 3, pp 264-272, issn 0888-7543Article

A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11LAMARTINE, J; PITAVAL, A; SOULARUE, P et al.Genomics (San Diego, Calif.). 2000, Vol 67, Num 2, pp 232-236, issn 0888-7543Article

Connexin46 mutations in autosomal dominant congenital cataractMACKAY, D; LONIDES, A; KIBAR, Z et al.American journal of human genetics. 1999, Vol 64, Num 5, pp 1357-1364, issn 0002-9297Article

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotypeD'AMOURS, G; KIBAR, Z; MATHONNET, G et al.Clinical genetics. 2012, Vol 81, Num 2, pp 128-141, issn 0009-9163, 14 p.Article

Identification of a new chemically induced allele (Lp^m1Jus) at the loop-tail locus : Morphology, histology, and genetic mappingKIBAR, Z; UNDERHILL, D. A; CANONNE-HERGAUX, F et al.Genomics (San Diego, Calif.). 2001, Vol 72, Num 3, pp 331-337, issn 0888-7543Article

Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous traitDUBE, M.-P; MLODZIENSKI, M. A; KIBAR, Z et al.American journal of human genetics. 1997, Vol 60, Num 3, pp 625-629, issn 0002-9297Article

The gene responsible for Clouston hidrotic ectodermal dysplasia maps for the pericentromeric region of chromosome 13qKIBAR, Z; DER KALOUSTIAN, V. M; BRAIS, B et al.Human molecular genetics (Print). 1996, Vol 5, Num 4, pp 543-547, issn 0964-6906Article