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J Jenderny

Showing results (11-20 of 24) with videos related to

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Human Genetics|April 1, 1992
Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20J Jenderny, J Gebauer, G Röhrborn, et al.
Journal of Medical Genetics|November 1, 1993
Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotypeJ Jenderny, A Caliebe, C Beyer, et al.
Hamostaseologie|August 4, 2010
FXIII deficiency due to base exchange Thr 449 (ACT) --> Ile (ATT) in exon 11 of the factor 13A gene. A cause of bleeding?B Maak, L Kochhan, P Heuchel, et al.
Human Genetics|September 1, 1992
Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patientsJ Jenderny, M L Jacobi, A Rüger, et al.
Mutation Research|February 1, 1988
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration. II. CyclophosphamideJ Jenderny, R A Walk, U Hackenberg, et al.
Mutation Research|December 1, 1987
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration: I. DiepoxybutaneR A Walk, J Jenderny, G Röhrborn, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1992
[Killian-Teschler-Nicola syndrome (Pallister-Killian syndrome, mosaic tetrasomy 12p)]R Pankau, U Diebold, J Jenderny, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Detection of a concomitant distal deletion in an inverted duplication of chromosome 3. Is there an overall mechanism for the origin of such duplications/deficiencies?J Jenderny, M Poetsch, M Hoeltzenbein, et al.
Nature|July 19, 1979
Aneuploidy in mouse fetuses after paternal exposure to x raysI Hansmann, R Zmarsly, H D Probeck, et al.
Human Genetics|December 1, 1995
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhoodJ Jenderny, E Köster, A Meyer, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Genetics|April 1, 1992
Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20J Jenderny, J Gebauer, G Röhrborn, et al.
Journal of Medical Genetics|November 1, 1993
Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotypeJ Jenderny, A Caliebe, C Beyer, et al.
Hamostaseologie|August 4, 2010
FXIII deficiency due to base exchange Thr 449 (ACT) --> Ile (ATT) in exon 11 of the factor 13A gene. A cause of bleeding?B Maak, L Kochhan, P Heuchel, et al.
Human Genetics|September 1, 1992
Chromosome aberrations in 450 sperm complements from eight controls and lack of increase after chemotherapy in two patientsJ Jenderny, M L Jacobi, A Rüger, et al.
Mutation Research|February 1, 1988
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration. II. CyclophosphamideJ Jenderny, R A Walk, U Hackenberg, et al.
Mutation Research|December 1, 1987
Chromosomal abnormalities and sister-chromatid exchange in bone marrow cells of mice and Chinese hamsters after inhalation and intraperitoneal administration: I. DiepoxybutaneR A Walk, J Jenderny, G Röhrborn, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1992
[Killian-Teschler-Nicola syndrome (Pallister-Killian syndrome, mosaic tetrasomy 12p)]R Pankau, U Diebold, J Jenderny, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Detection of a concomitant distal deletion in an inverted duplication of chromosome 3. Is there an overall mechanism for the origin of such duplications/deficiencies?J Jenderny, M Poetsch, M Hoeltzenbein, et al.
Nature|July 19, 1979
Aneuploidy in mouse fetuses after paternal exposure to x raysI Hansmann, R Zmarsly, H D Probeck, et al.
Human Genetics|December 1, 1995
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhoodJ Jenderny, E Köster, A Meyer, et al.
Pageof 3