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V Kalatzis

Showing results (11-20 of 16) with videos related to

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Human Genetics|April 1, 1992
The gene for the human IgA Fc receptor maps to 19q13.4E J Kremer, V Kalatzis, E Baker, 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.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Human Genetics|April 1, 1992
The gene for the human IgA Fc receptor maps to 19q13.4E J Kremer, V Kalatzis, E Baker, 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.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 2