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T Grimm

Showing results (41-50 of 143) with videos related to

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Journal of Medical Genetics|May 1, 1989
Benign muscular dystrophy: risk calculation in families with consanguinityG Wolff, C R Müller, T Grimm
Annales De Genetique|January 1, 1983
Partial trisomy 7q in two siblingsM Klasen, M Schmid, I Hansmann, et al.
Cytogenetics and Cell Genetics|February 15, 2001
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephalyW Kress, B Petersen, H Collmann, et al.
Prenatal Diagnosis|September 1, 1986
Prenatal diagnosis of a complex, balanced rearrangement of chromosomes 7 and 14 in a healthy child with a history of preconceptual X-ray exposureJ Köhler, M Brackertz, A Feige, et al.
ACS Applied Materials & Interfaces|January 22, 2021
Unique Degradation Signatures of Organic Solar Cells with Nonfullerene Electron AcceptorsPranab Deb, Ryan T Grimm, John K Grey
Klinische Padiatrie|January 1, 1985
[Holoprosencephaly--clinical picture and genetic counseling in 6 cases]M Brackertz, D Schindler, T Grimm, et al.
American Journal of Medical Genetics|February 1, 1988
Theoretical expectations for deletional mutations in Duchenne muscular dystrophyT Grimm, G A Danieli, C R Muller
Zentralblatt Fur Neurochirurgie|September 8, 2006
Genetics of cerebral cavernous angiomaU Felbor, U Sure, T Grimm, et al.
American Journal of Medical Genetics|October 1, 1988
Prenatal exclusion of Norrie disease with flanking DNA markersA Gal, S Uhlhaas, D Glaser, et al.
Experimental Cell Research|July 1, 1978
Onset of nucleolus organizer activity in early mouse embryogenesis and evidence for its regulationI Hansmann, J Gebauer, L Bihl, et al.
Pageof 15

Showing results (41-50 of 143) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|May 1, 1989
Benign muscular dystrophy: risk calculation in families with consanguinityG Wolff, C R Müller, T Grimm
Annales De Genetique|January 1, 1983
Partial trisomy 7q in two siblingsM Klasen, M Schmid, I Hansmann, et al.
Cytogenetics and Cell Genetics|February 15, 2001
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephalyW Kress, B Petersen, H Collmann, et al.
Prenatal Diagnosis|September 1, 1986
Prenatal diagnosis of a complex, balanced rearrangement of chromosomes 7 and 14 in a healthy child with a history of preconceptual X-ray exposureJ Köhler, M Brackertz, A Feige, et al.
ACS Applied Materials & Interfaces|January 22, 2021
Unique Degradation Signatures of Organic Solar Cells with Nonfullerene Electron AcceptorsPranab Deb, Ryan T Grimm, John K Grey
Klinische Padiatrie|January 1, 1985
[Holoprosencephaly--clinical picture and genetic counseling in 6 cases]M Brackertz, D Schindler, T Grimm, et al.
American Journal of Medical Genetics|February 1, 1988
Theoretical expectations for deletional mutations in Duchenne muscular dystrophyT Grimm, G A Danieli, C R Muller
Zentralblatt Fur Neurochirurgie|September 8, 2006
Genetics of cerebral cavernous angiomaU Felbor, U Sure, T Grimm, et al.
American Journal of Medical Genetics|October 1, 1988
Prenatal exclusion of Norrie disease with flanking DNA markersA Gal, S Uhlhaas, D Glaser, et al.
Experimental Cell Research|July 1, 1978
Onset of nucleolus organizer activity in early mouse embryogenesis and evidence for its regulationI Hansmann, J Gebauer, L Bihl, et al.
Pageof 15