A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2156
- 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 de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle ; volume:18 ; number:1 ; day:2 ; month:8 ; year:2017 ; pages:1-9 ; date:12.2017
BMC genetics ; 18, Heft 1 (2.8.2017), 1-9, 12.2017
- Classification
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Landwirtschaft, Veterinärmedizin
- Creator
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Agerholm, JøRgen S.
- Contributor
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McEvoy, Fintan J.
Heegaard, Steffen
Charlier, Carole
Jagannathan, Vidhya
Drögemüller, Cord
SpringerLink (Online service)
- DOI
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10.1186/s12863-017-0541-3
- URN
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urn:nbn:de:1111-2017101814656
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:32 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
- Agerholm, JøRgen S.
- McEvoy, Fintan J.
- Heegaard, Steffen
- Charlier, Carole
- Jagannathan, Vidhya
- Drögemüller, Cord
- SpringerLink (Online service)
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A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
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Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia
A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter release
A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle
SOAT1 missense variant in two cats with sebaceous gland dysplasia
Metaphyseal dysplasia associated with chronic facial nerve palsy
A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia
A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
Perinatal Autopsy Findings in a Case of De Novo Hypohidrotic Ectodermal Dysplasia
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A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter release