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Human Molecular Genetics|September 15, 1998
The fundamental and medical impacts of recent progress in research on hereditary hearing lossV Kalatzis, C PetitDevelopmental Dynamics : an Official Publication of the American Association of Anatomists|December 16, 1998
Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndromeV Kalatzis, I Sahly, A El-Amraoui, et al.Genomics|June 15, 1996
Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndromeV Kalatzis, S Abdelhak, S Compain, et al.European Journal of Human Genetics : EJHG|July 1, 1997
BOR and BO syndromes are allelic defects of EYA1C Vincent, V Kalatzis, S Abdelhak, et al.Cancer Genetics and Cytogenetics|September 1, 1993
Mapping of the chromosome 11 breakpoint of the t(4;11)(q21;p14-15) translocationV Kalatzis, G B Peters, A DobrovicThe Journal of Biological Chemistry|January 21, 2001
The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motifS Cherqui, V Kalatzis, G Trugnan, et al.The EMBO Journal|November 2, 2001
Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporterV Kalatzis, S Cherqui, C Antignac, et al.BMC Genomics|December 20, 2000
Identification and characterisation of the murine homologue of the gene responsible for cystinosis, CtnsS Cherqui, V Kalatzis, L Forestier, et al.Annual Review of Genomics and Human Genetics|November 10, 2001
Usher syndrome: from genetics to pathogenesisC PetitTrends in Endocrinology and Metabolism: TEM|January 1, 1993
Molecular basis of the X-chromosome-linked Kallmann's syndromeC PetitPageof 47