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A A Bergen

Showing results (1-10 of 59) with videos related to

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American Journal of Human Genetics|June 1, 1997
Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneityA A Bergen, A J Pinckers
American Journal of Human Genetics|October 3, 1998
Reply to InglehearnA A Bergen, A J Pinckers
Journal of Medical Genetics|July 1, 1994
Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOBA A Bergen, P Kestelyn, M Leys, et al.
Clinical Genetics|May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophyA A Bergen, F Meire, E J Schuurman, et al.
The British Journal of Ophthalmology|July 1, 1995
Efficient DNA carrier detection in X linked juvenile retinoschisisA A Bergen, J B ten Brink, M J van Schooneveld
Nucleic Acids Research|July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12B Arveiler, M H Hofker, A A Bergen, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1992
A retrospective study of registered retinitis pigmentosa patients in The NetherlandsL I van den Born, A A Bergen, E M Bleeker-Wagemakers
Genomics|May 1, 1994
Nance-Horan syndrome: linkage analysis in a family from The NetherlandsA A Bergen, J ten Brink, E J Schuurman, et al.
Genetic Epidemiology|January 1, 1995
Maximum-likelihood estimation in linkage heterogeneity models including additional information via the EM algorithmJ J Houwing-Duistermaat, L A Sandkuijl, A A Bergen, et al.
The British Journal of Ophthalmology|February 1, 1994
X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysisF M Meire, A A Bergen, A De Rouck, et al.
Pageof 6

Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|June 1, 1997
Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneityA A Bergen, A J Pinckers
American Journal of Human Genetics|October 3, 1998
Reply to InglehearnA A Bergen, A J Pinckers
Journal of Medical Genetics|July 1, 1994
Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOBA A Bergen, P Kestelyn, M Leys, et al.
Clinical Genetics|May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophyA A Bergen, F Meire, E J Schuurman, et al.
The British Journal of Ophthalmology|July 1, 1995
Efficient DNA carrier detection in X linked juvenile retinoschisisA A Bergen, J B ten Brink, M J van Schooneveld
Nucleic Acids Research|July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12B Arveiler, M H Hofker, A A Bergen, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1992
A retrospective study of registered retinitis pigmentosa patients in The NetherlandsL I van den Born, A A Bergen, E M Bleeker-Wagemakers
Genomics|May 1, 1994
Nance-Horan syndrome: linkage analysis in a family from The NetherlandsA A Bergen, J ten Brink, E J Schuurman, et al.
Genetic Epidemiology|January 1, 1995
Maximum-likelihood estimation in linkage heterogeneity models including additional information via the EM algorithmJ J Houwing-Duistermaat, L A Sandkuijl, A A Bergen, et al.
The British Journal of Ophthalmology|February 1, 1994
X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysisF M Meire, A A Bergen, A De Rouck, et al.
Pageof 6