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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Z Kibar

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The British Journal of Dermatology|March 24, 2000

Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French familyJ Lamartine, D Laoudj, C Blanchet-Bardon, et al.

Clinical Genetics|August 27, 2010

Contribution of VANGL2 mutations to isolated neural tube defectsZ Kibar, S Salem, C M Bosoi, et al.

American Journal of Human Genetics|March 1, 1997

Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous traitM P Dubé, M A Mlodzienski, Z Kibar, et al.

Gene|November 25, 1997

Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3R G Lafrenière, Z Kibar, D L Rochefort, et al.

Genomics|December 15, 1996

Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3R G Lafrenière, D L Rochefort, Z Kibar, et al.

Nature Genetics|October 4, 2000

Mutations in GJB6 cause hidrotic ectodermal dysplasiaJ Lamartine, G Munhoz Essenfelder, Z Kibar, et al.

European Journal of Human Genetics : EJHG|June 15, 2000

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.

Pageof 2

Search research articles

Showing results (11-20 of 17) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 17 results.

The British Journal of Dermatology|March 24, 2000

Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French familyJ Lamartine, D Laoudj, C Blanchet-Bardon, et al.

Clinical Genetics|August 27, 2010

Contribution of VANGL2 mutations to isolated neural tube defectsZ Kibar, S Salem, C M Bosoi, et al.

American Journal of Human Genetics|March 1, 1997

Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous traitM P Dubé, M A Mlodzienski, Z Kibar, et al.

Gene|November 25, 1997

Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3R G Lafrenière, Z Kibar, D L Rochefort, et al.

Genomics|December 15, 1996

Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3R G Lafrenière, D L Rochefort, Z Kibar, et al.

Nature Genetics|October 4, 2000

Mutations in GJB6 cause hidrotic ectodermal dysplasiaJ Lamartine, G Munhoz Essenfelder, Z Kibar, et al.

European Journal of Human Genetics : EJHG|June 15, 2000

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.

Pageof 2