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J Weissenbach

Showing results (161-170 of 363) with videos related to

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Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Genomics|September 15, 1994
Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3P A Farndon, D J Morris, C Hardy, et al.
American Journal of Human Genetics|April 1, 1994
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5qL van Herwerden, C S Rose, W Reardon, et al.
Circulation Research|October 1, 1995
An isolated cardiac conduction disease maps to chromosome 19qA de Meeus, E Stephan, S Debrus, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1995
Readjusting the localization of long QT syndrome gene on chromosome 11p15E Dausse, I Denjoy, P Kahlem, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 20V Wunderle, C Dib, C Fizames, et al.
Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
American Journal of Human Genetics|January 1, 1995
Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414A Sander, J C Murray, T Scherpbier-Heddema, et al.
Human Molecular Genetics|July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22H Chaib, C Place, N Salem, et al.
Pageof 37

Showing results (161-170 of 363) with videos related to

Sort By:
Pageof 37
Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Genomics|September 15, 1994
Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3P A Farndon, D J Morris, C Hardy, et al.
American Journal of Human Genetics|April 1, 1994
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5qL van Herwerden, C S Rose, W Reardon, et al.
Circulation Research|October 1, 1995
An isolated cardiac conduction disease maps to chromosome 19qA de Meeus, E Stephan, S Debrus, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1995
Readjusting the localization of long QT syndrome gene on chromosome 11p15E Dausse, I Denjoy, P Kahlem, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 20V Wunderle, C Dib, C Fizames, et al.
Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
American Journal of Human Genetics|January 1, 1995
Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414A Sander, J C Murray, T Scherpbier-Heddema, et al.
Human Molecular Genetics|July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22H Chaib, C Place, N Salem, et al.
Pageof 37