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E Passarge

Showing results (141-150 of 151) with videos related to

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American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Nature|July 22, 1976
Benzpyrene induces sister chromatid exchanges in cultured human lymphocytesH W Rudiger, F Kohl, W Mangels, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Journal of Reproductive Immunology|July 1, 1991
Fc receptor blocking antibodies after active immunization for the treatment of recurrent spontaneous abortionU Kuhn, R Blasczyk, B Hojnacki, et al.
American Journal of Medical Genetics|March 1, 1989
Further delineation of the Nijmegen breakage syndromeR D Taalman, T W Hustinx, C M Weemaes, et al.
Prenatal Diagnosis|February 1, 1988
HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAHH Grosse-Wilde, E Valentine-Thon, U Vögeler, et al.
American Journal of Human Genetics|November 1, 1977
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the AshkenazimJ German, D Bloom, E Passarge, et al.
Clinical Genetics|February 1, 1990
Use of the RB1 cDNA as a diagnostic probe in retinoblastoma familiesA D Goddard, R A Phillips, V Greger, et al.
Nature|December 26, 1970
Triosephosphate isomerase gene not localized on the short arm of chromosome 5 in manH W Rüdiger, E Passarge, L Hirth, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 16

Showing results (141-150 of 151) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Nature|July 22, 1976
Benzpyrene induces sister chromatid exchanges in cultured human lymphocytesH W Rudiger, F Kohl, W Mangels, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Journal of Reproductive Immunology|July 1, 1991
Fc receptor blocking antibodies after active immunization for the treatment of recurrent spontaneous abortionU Kuhn, R Blasczyk, B Hojnacki, et al.
American Journal of Medical Genetics|March 1, 1989
Further delineation of the Nijmegen breakage syndromeR D Taalman, T W Hustinx, C M Weemaes, et al.
Prenatal Diagnosis|February 1, 1988
HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAHH Grosse-Wilde, E Valentine-Thon, U Vögeler, et al.
American Journal of Human Genetics|November 1, 1977
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the AshkenazimJ German, D Bloom, E Passarge, et al.
Clinical Genetics|February 1, 1990
Use of the RB1 cDNA as a diagnostic probe in retinoblastoma familiesA D Goddard, R A Phillips, V Greger, et al.
Nature|December 26, 1970
Triosephosphate isomerase gene not localized on the short arm of chromosome 5 in manH W Rüdiger, E Passarge, L Hirth, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 16