A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2164
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle ; volume:17 ; number:1 ; day:25 ; month:5 ; year:2016 ; pages:1-13 ; date:12.2016
BMC genomics ; 17, Heft 1 (25.5.2016), 1-13, 12.2016
- Creator
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Schwarzenbacher, Hermann
- Contributor
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Burgstaller, Johann
Seefried, Franz R.
Wurmser, Christine
Hilbe, Monika
Jung, Simone
Fuerst, Christian
Dinhopl, Nora
Weissenböck, Herbert
Fuerst-Waltl, Birgit
Dolezal, Marlies
Winkler, Reinhard
Grueter, Oskar
Bleul, Ulrich
Wittek, Thomas
Fries, Ruedi
Pausch, Hubert
SpringerLink (Online service)
- DOI
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10.1186/s12864-016-2742-y
- URN
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urn:nbn:de:1111-201605275713
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Schwarzenbacher, Hermann
- Burgstaller, Johann
- Seefried, Franz R.
- Wurmser, Christine
- Hilbe, Monika
- Jung, Simone
- Fuerst, Christian
- Dinhopl, Nora
- Weissenböck, Herbert
- Fuerst-Waltl, Birgit
- Dolezal, Marlies
- Winkler, Reinhard
- Grueter, Oskar
- Bleul, Ulrich
- Wittek, Thomas
- Fries, Ruedi
- Pausch, Hubert
- SpringerLink (Online service)
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A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle
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Imputation of high-density genotypes in the Fleckvieh cattle population
Charakterisierung neuer Missense Mutationen im Lipidtransporter ABCA3
A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle
Fleckvieh
A missense mutation in Lama3 causes androgen alopecia
A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle
Rabson Mendenhall Syndrome caused by a novel missense mutation
Zuchtwertschätzung Fleckvieh
Visual evaluation of Simmental-Fleckvieh cattle
A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle
A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle
A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle
Imputation of high-density genotypes in the Fleckvieh cattle population
Charakterisierung neuer Missense Mutationen im Lipidtransporter ABCA3
A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle
Fleckvieh
A missense mutation in Lama3 causes androgen alopecia
A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle
Rabson Mendenhall Syndrome caused by a novel missense mutation
Zuchtwertschätzung Fleckvieh
Visual evaluation of Simmental-Fleckvieh cattle
A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle
A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle
A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle
Imputation of high-density genotypes in the Fleckvieh cattle population
Charakterisierung neuer Missense Mutationen im Lipidtransporter ABCA3
A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle
Fleckvieh
A missense mutation in Lama3 causes androgen alopecia
A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle
Rabson Mendenhall Syndrome caused by a novel missense mutation