Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C M Aalfs

Showing results (1-10 of 43) with videos related to

Pageof 5
Sort By:
American Journal of Medical Genetics|September 25, 1995
Differences between the Hoyeraal-Hreidarsson syndrome and an autosomal recessive congenital intrauterine infection-like syndromeC M Aalfs, R C Hennekam
Nederlands Tijdschrift Voor Geneeskunde|February 4, 2005
[DNA-analysis in hereditary cancer: the importance of a reliable family history]S Kapma, N J Leschot, C M Aalfs
American Journal of Medical Genetics|September 24, 1999
Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndromeC M Aalfs, J M Hoovers, F A Wijburg
Community Genetics|June 19, 2007
Genetic counselling for familial conditions during pregnancy: a review of the literature published during the years 1989-2004C M Aalfs, E M A Smets, N J Leschot
Nederlands Tijdschrift Voor Geneeskunde|June 8, 2017
[Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients]C M Aalfs, A M Westermann, C G van El
Nederlands Tijdschrift Voor Geneeskunde|September 6, 2001
[Prenatal genetic counseling in pregnancy: the importance of (early) timely referral ]C M Aalfs, E M Smets, J C de Haes, et al.
European Journal of Pediatrics|April 1, 1995
The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasiaC M Aalfs, H van den Berg, P G Barth, et al.
American Journal of Medical Genetics|March 29, 1996
Further delineation of the acro-renal-ocular syndromeC M Aalfs, M J van Schooneveld, E M van Keulen, et al.
Human Mutation|February 6, 1998
Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasiaP P Deutz-Terlouw, M Losekoot, C M Aalfs, et al.
Electroencephalography and Clinical Neurophysiology|December 1, 1993
Posterior tibial and sural nerve somatosensory evoked potentials: a study in spastic paraparesis and spinal cord lesionsC M Aalfs, J H Koelman, F E Posthumus Meyjes, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|September 25, 1995
Differences between the Hoyeraal-Hreidarsson syndrome and an autosomal recessive congenital intrauterine infection-like syndromeC M Aalfs, R C Hennekam
Nederlands Tijdschrift Voor Geneeskunde|February 4, 2005
[DNA-analysis in hereditary cancer: the importance of a reliable family history]S Kapma, N J Leschot, C M Aalfs
American Journal of Medical Genetics|September 24, 1999
Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndromeC M Aalfs, J M Hoovers, F A Wijburg
Community Genetics|June 19, 2007
Genetic counselling for familial conditions during pregnancy: a review of the literature published during the years 1989-2004C M Aalfs, E M A Smets, N J Leschot
Nederlands Tijdschrift Voor Geneeskunde|June 8, 2017
[Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients]C M Aalfs, A M Westermann, C G van El
Nederlands Tijdschrift Voor Geneeskunde|September 6, 2001
[Prenatal genetic counseling in pregnancy: the importance of (early) timely referral ]C M Aalfs, E M Smets, J C de Haes, et al.
European Journal of Pediatrics|April 1, 1995
The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasiaC M Aalfs, H van den Berg, P G Barth, et al.
American Journal of Medical Genetics|March 29, 1996
Further delineation of the acro-renal-ocular syndromeC M Aalfs, M J van Schooneveld, E M van Keulen, et al.
Human Mutation|February 6, 1998
Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasiaP P Deutz-Terlouw, M Losekoot, C M Aalfs, et al.
Electroencephalography and Clinical Neurophysiology|December 1, 1993
Posterior tibial and sural nerve somatosensory evoked potentials: a study in spastic paraparesis and spinal cord lesionsC M Aalfs, J H Koelman, F E Posthumus Meyjes, et al.
Pageof 5