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C M Aalfs

Showing results (11-20 of 43) with videos related to

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American Journal of Human Genetics|April 1, 1997
Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblastsE A Putnam, E S Park, C M Aalfs, et al.
Human Mutation|June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basisC M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
Clinical Genetics|January 1, 1996
Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delayC M Aalfs, M E Jacobs, M A Nieste-Otter, et al.
Neuroscience and Biobehavioral Reviews|December 10, 2020
Polygenic risk scores for genetic counseling in psychiatry: Lessons learned from other fields of medicineE Eeltink, M Z van der Horst, J R Zinkstok, et al.
Familial Cancer|March 25, 2015
Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancerF G J Kallenberg, J E G IJspeert, P M M Bossuyt, et al.
Tijdschrift Voor Psychiatrie|June 23, 2022
[Genetic risk of mental illness: what do we know and how do we communicate this?]J R Zinkstok, M Z van der Horst, R P H Wouters, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 13, 1996
[Smith-Lemli-Opitz syndrome; a special defect in cholesterol metabolism]C M Aalfs, R C Hennekam, R J Wanders, et al.
Tijdschrift Voor Psychiatrie|June 23, 2022
[Guidelines on genetic testing in psychiatry: an overview]M Z van der Horst, C M Aalfs, J A S Vorstman, et al.
Journal of Neurology|June 1, 1993
Posterior tibial nerve somatosensory evoked potentials in slowly progressive spastic paraplegia: a comparative study with clinical signsC M Aalfs, J H Koelman, M Aramideh, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 15, 1995
[Wilson's disease; diagnosis with the aid of magnetic resonance tomography]J S van den Berg, T U Hoogenraad, J A Duyn, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|April 1, 1997
Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblastsE A Putnam, E S Park, C M Aalfs, et al.
Human Mutation|June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basisC M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
Clinical Genetics|January 1, 1996
Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delayC M Aalfs, M E Jacobs, M A Nieste-Otter, et al.
Neuroscience and Biobehavioral Reviews|December 10, 2020
Polygenic risk scores for genetic counseling in psychiatry: Lessons learned from other fields of medicineE Eeltink, M Z van der Horst, J R Zinkstok, et al.
Familial Cancer|March 25, 2015
Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancerF G J Kallenberg, J E G IJspeert, P M M Bossuyt, et al.
Tijdschrift Voor Psychiatrie|June 23, 2022
[Genetic risk of mental illness: what do we know and how do we communicate this?]J R Zinkstok, M Z van der Horst, R P H Wouters, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 13, 1996
[Smith-Lemli-Opitz syndrome; a special defect in cholesterol metabolism]C M Aalfs, R C Hennekam, R J Wanders, et al.
Tijdschrift Voor Psychiatrie|June 23, 2022
[Guidelines on genetic testing in psychiatry: an overview]M Z van der Horst, C M Aalfs, J A S Vorstman, et al.
Journal of Neurology|June 1, 1993
Posterior tibial nerve somatosensory evoked potentials in slowly progressive spastic paraplegia: a comparative study with clinical signsC M Aalfs, J H Koelman, M Aramideh, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 15, 1995
[Wilson's disease; diagnosis with the aid of magnetic resonance tomography]J S van den Berg, T U Hoogenraad, J A Duyn, et al.
Pageof 5