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C Hamel

Showing results (211-220 of 291) with videos related to

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Nature Genetics|March 1, 1994
A complex bilateral polysyndactyly disease locus maps to chromosome 7q36O Tsukurov, A Boehmer, J Flynn, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Acta Obstetricia Et Gynecologica Scandinavica|July 10, 2021
Diagnostic criteria for retained products of conception-A scoping reviewCharlotte C Hamel, Steffi van Wessel, Alasdair Carnegy, et al.
Journal of Neurology|November 29, 2005
Recurrent neuropathy associated with Ehlers-Danlos syndromeN C Voermans, G Drost, A van Kampen, et al.
American Journal of Medical Genetics|February 25, 1998
Pfeiffer syndrome type 2: further delineation and review of the literatureA S Plomp, B C Hamel, J M Cobben, et al.
Human Molecular Genetics|April 1, 1995
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardationD Kotzot, S Schmitt, F Bernasconi, et al.
The Cochrane Database of Systematic Reviews|July 20, 2007
WITHDRAWN: Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
The Cochrane Database of Systematic Reviews|October 30, 2003
Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
The Cochrane Database of Systematic Reviews|February 20, 2004
Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
Annals of the New York Academy of Sciences|June 8, 1996
A mutation in COL9A2 causes multiple epiphyseal dysplasia (EDM2)Y Muragaki, E C Mariman, S E van Beersum, et al.
Pageof 30

Showing results (211-220 of 291) with videos related to

Sort By:
Pageof 30
Nature Genetics|March 1, 1994
A complex bilateral polysyndactyly disease locus maps to chromosome 7q36O Tsukurov, A Boehmer, J Flynn, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Acta Obstetricia Et Gynecologica Scandinavica|July 10, 2021
Diagnostic criteria for retained products of conception-A scoping reviewCharlotte C Hamel, Steffi van Wessel, Alasdair Carnegy, et al.
Journal of Neurology|November 29, 2005
Recurrent neuropathy associated with Ehlers-Danlos syndromeN C Voermans, G Drost, A van Kampen, et al.
American Journal of Medical Genetics|February 25, 1998
Pfeiffer syndrome type 2: further delineation and review of the literatureA S Plomp, B C Hamel, J M Cobben, et al.
Human Molecular Genetics|April 1, 1995
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardationD Kotzot, S Schmitt, F Bernasconi, et al.
The Cochrane Database of Systematic Reviews|July 20, 2007
WITHDRAWN: Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
The Cochrane Database of Systematic Reviews|October 30, 2003
Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
The Cochrane Database of Systematic Reviews|February 20, 2004
Calcium supplementation on bone loss in postmenopausal womenB Shea, G Wells, A Cranney, et al.
Annals of the New York Academy of Sciences|June 8, 1996
A mutation in COL9A2 causes multiple epiphyseal dysplasia (EDM2)Y Muragaki, E C Mariman, S E van Beersum, et al.
Pageof 30