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B Hove

Showing results (41-50 of 56) with videos related to

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European Journal of Medical Genetics|June 16, 2018
Aortic aneurysm: An underestimated serious finding in the EP300 mutation phenotypical spectrumIlse Luyckx, Nikhita Bolar, Birgitte Rode Diness, et al.
Biochemical Society Transactions|November 1, 1995
Are all four yeast PRS genes essential?A T Carter, F Beiche, A Narbad, et al.
Acta Neurochirurgica|January 1, 1989
Per- and postoperative changes in the arterio-venous oxygen content difference (AVDO2) in patients subjected to craniotomy for cerebral tumoursJ Asmussen, S Elkjaer, G Cold, et al.
Clinical Case Reports|July 7, 2017
Prenatal diagnosis of autosomal recessive Robinow syndrome using 3D ultrasoundBolette F Jeppesen, Hanne B Hove, Sven Kreiborg, et al.
Clinical Dysmorphology|September 27, 2018
Novel de novo mutation in ZBTB20 in primrose syndrome in boy with short statureSigrún Grímsdóttir, Hanne B Hove, Sven Kreiborg, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 24, 2020
Facial Asymmetry in Nonsyndromic and Muenke Syndrome-Associated Unicoronal Synostosis: A 3-Dimensional Study Based on Facial Surfaces Extracted From CT ScansLouise Öwall, Tron A Darvann, Hanne B Hove, et al.
Molecular & General Genetics : MGG|March 26, 1997
PRS1 is a key member of the gene family encoding phosphoribosylpyrophosphate synthetase in Saccharomyces cerevisiaeA T Carter, F Beiche, B Hove-Jensen, et al.
Calcified Tissue International|September 7, 2019
Multiple Fractures and Impaired Bone Fracture Healing in a Patient with Pycnodysostosis and HypophosphatasiaNicola Hepp, Anja Lisbeth Frederiksen, Morten Dunø, et al.
Archives of Disease in Childhood|July 17, 2025
Sleep-disordered breathing in children with achondroplasia assessed by polysomnography: a retrospective chart reviewLouise Hove Buciek, Jeppe Ravn Jacobsen, Supriya Raj, et al.
European Journal of Endocrinology|May 18, 2026
Navepegritide Combined with Lonapegsomatropin for the Treatment of Children with Achondroplasia: 52-Week Results from the Phase 2 COACH TrialCiara M McDonnell, Melita Irving, Line Aagaard Nolting, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
European Journal of Medical Genetics|June 16, 2018
Aortic aneurysm: An underestimated serious finding in the EP300 mutation phenotypical spectrumIlse Luyckx, Nikhita Bolar, Birgitte Rode Diness, et al.
Biochemical Society Transactions|November 1, 1995
Are all four yeast PRS genes essential?A T Carter, F Beiche, A Narbad, et al.
Acta Neurochirurgica|January 1, 1989
Per- and postoperative changes in the arterio-venous oxygen content difference (AVDO2) in patients subjected to craniotomy for cerebral tumoursJ Asmussen, S Elkjaer, G Cold, et al.
Clinical Case Reports|July 7, 2017
Prenatal diagnosis of autosomal recessive Robinow syndrome using 3D ultrasoundBolette F Jeppesen, Hanne B Hove, Sven Kreiborg, et al.
Clinical Dysmorphology|September 27, 2018
Novel de novo mutation in ZBTB20 in primrose syndrome in boy with short statureSigrún Grímsdóttir, Hanne B Hove, Sven Kreiborg, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 24, 2020
Facial Asymmetry in Nonsyndromic and Muenke Syndrome-Associated Unicoronal Synostosis: A 3-Dimensional Study Based on Facial Surfaces Extracted From CT ScansLouise Öwall, Tron A Darvann, Hanne B Hove, et al.
Molecular & General Genetics : MGG|March 26, 1997
PRS1 is a key member of the gene family encoding phosphoribosylpyrophosphate synthetase in Saccharomyces cerevisiaeA T Carter, F Beiche, B Hove-Jensen, et al.
Calcified Tissue International|September 7, 2019
Multiple Fractures and Impaired Bone Fracture Healing in a Patient with Pycnodysostosis and HypophosphatasiaNicola Hepp, Anja Lisbeth Frederiksen, Morten Dunø, et al.
Archives of Disease in Childhood|July 17, 2025
Sleep-disordered breathing in children with achondroplasia assessed by polysomnography: a retrospective chart reviewLouise Hove Buciek, Jeppe Ravn Jacobsen, Supriya Raj, et al.
European Journal of Endocrinology|May 18, 2026
Navepegritide Combined with Lonapegsomatropin for the Treatment of Children with Achondroplasia: 52-Week Results from the Phase 2 COACH TrialCiara M McDonnell, Melita Irving, Line Aagaard Nolting, et al.
Pageof 6