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A Eigel

Showing results (21-30 of 35) with videos related to

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Human Genetics|September 1, 1996
Prevalence of alpha-thalassemias in northern ThailandM Lemmens-Zygulska, A Eigel, B Helbig, et al.
Human Genetics|November 1, 1991
Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutationsM Zygulska, A Eigel, B Dworniczak, et al.
Deutsche Medizinische Wochenschrift (1946)|May 7, 1993
[Mutation in the cystic fibrosis transmembrane-regulator gene in bilateral congenital ductus deferens aplasia]D Meschede, C Keck, C De Geyter, et al.
Human Genetics|January 1, 1987
Hemoglobin M Iwate is caused by a C----T transition in codon 87 of the human alpha 1-globin geneJ Horst, G Assum, E U Griese, et al.
Human Mutation|February 5, 2000
Different ocular abnormalities in individuals of a three-generation family caused by a new nonsense mutation in the PST domain of the PAX6 gene. Mutations in brief no. 189. OnlineY Syagailo, K Wilke, O Okladnova, et al.
Human Mutation|December 19, 2001
Seven novel and four recurrent point mutations in the factor VIII (F8C) geneN Bogdanova, B Lemcke, A Markoff, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Zoology (Jena, Germany)|November 1, 2023
Land Ho! Polarized light serves as a visual signal for landward orientation in displaced spidersSidney J Goedeker, Nettie A Eigel, Madeline R Mann, et al.
Human Genetics|December 1, 1988
Cystic fibrosis: typing 89 German families with linked DNA probesJ Weber, C Aulehla-Scholz, R Kaiser, et al.
American Journal of Human Genetics|July 1, 1989
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia BM Ludwig, R Schwaab, A Eigel, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Human Genetics|September 1, 1996
Prevalence of alpha-thalassemias in northern ThailandM Lemmens-Zygulska, A Eigel, B Helbig, et al.
Human Genetics|November 1, 1991
Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutationsM Zygulska, A Eigel, B Dworniczak, et al.
Deutsche Medizinische Wochenschrift (1946)|May 7, 1993
[Mutation in the cystic fibrosis transmembrane-regulator gene in bilateral congenital ductus deferens aplasia]D Meschede, C Keck, C De Geyter, et al.
Human Genetics|January 1, 1987
Hemoglobin M Iwate is caused by a C----T transition in codon 87 of the human alpha 1-globin geneJ Horst, G Assum, E U Griese, et al.
Human Mutation|February 5, 2000
Different ocular abnormalities in individuals of a three-generation family caused by a new nonsense mutation in the PST domain of the PAX6 gene. Mutations in brief no. 189. OnlineY Syagailo, K Wilke, O Okladnova, et al.
Human Mutation|December 19, 2001
Seven novel and four recurrent point mutations in the factor VIII (F8C) geneN Bogdanova, B Lemcke, A Markoff, et al.
Journal of Medical Genetics|December 1, 1990
Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutationsL Kalaydjieva, B Dworniczak, C Aulehla-Scholz, et al.
Zoology (Jena, Germany)|November 1, 2023
Land Ho! Polarized light serves as a visual signal for landward orientation in displaced spidersSidney J Goedeker, Nettie A Eigel, Madeline R Mann, et al.
Human Genetics|December 1, 1988
Cystic fibrosis: typing 89 German families with linked DNA probesJ Weber, C Aulehla-Scholz, R Kaiser, et al.
American Journal of Human Genetics|July 1, 1989
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia BM Ludwig, R Schwaab, A Eigel, et al.
Pageof 4