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I Feenstra

Showing results (1-10 of 12) with videos related to

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Cytogenetic and Genome Research|November 25, 2006
Cytogenetic genotype-phenotype studies: improving genotyping, phenotyping and data storageI Feenstra, H G Brunner, C M A van Ravenswaaij
Clinical Genetics|February 20, 2014
Genotype phenotype correlations for hearing impairment: approaches to managementL H Hoefsloot, I Feenstra, H P M Kunst, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 13, 2016
Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomaliesL Beulen, B H W Faas, I Feenstra, et al.
Neuropediatrics|June 15, 2006
Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8I Feenstra, C M A van Ravenswaaij, M S van der Knaap, et al.
International Journal of Epidemiology|December 1, 1978
Should we screen all newborns for cystic fibrosis?L P Ten Kate, I Feenstra-de Gooyer, G Ploeg-de Groot, et al.
Clinical Genetics|May 28, 2014
Patient experiences with gene panels based on exome sequencing in clinical diagnostics: high acceptance and low distressA S Sie, J B Prins, W A G van Zelst-Stams, et al.
Human Reproduction Update|September 30, 2006
Globozoospermia revisitedA H D M Dam, I Feenstra, J R Westphal, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Neuropsychiatry and deletions of 18q; case report and diagnostic considerationsW M A Verhoeven, I Feenstra, C Van Ravenswaay-Arts, et al.
European Journal of Medical Genetics|March 1, 2006
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literatureI Feenstra, D A Koolen, J Van der Pas, et al.
European Journal of Medical Genetics|July 11, 2006
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalitiesI Feenstra, J Fang, D A Koolen, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Cytogenetic and Genome Research|November 25, 2006
Cytogenetic genotype-phenotype studies: improving genotyping, phenotyping and data storageI Feenstra, H G Brunner, C M A van Ravenswaaij
Clinical Genetics|February 20, 2014
Genotype phenotype correlations for hearing impairment: approaches to managementL H Hoefsloot, I Feenstra, H P M Kunst, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 13, 2016
Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomaliesL Beulen, B H W Faas, I Feenstra, et al.
Neuropediatrics|June 15, 2006
Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8I Feenstra, C M A van Ravenswaaij, M S van der Knaap, et al.
International Journal of Epidemiology|December 1, 1978
Should we screen all newborns for cystic fibrosis?L P Ten Kate, I Feenstra-de Gooyer, G Ploeg-de Groot, et al.
Clinical Genetics|May 28, 2014
Patient experiences with gene panels based on exome sequencing in clinical diagnostics: high acceptance and low distressA S Sie, J B Prins, W A G van Zelst-Stams, et al.
Human Reproduction Update|September 30, 2006
Globozoospermia revisitedA H D M Dam, I Feenstra, J R Westphal, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Neuropsychiatry and deletions of 18q; case report and diagnostic considerationsW M A Verhoeven, I Feenstra, C Van Ravenswaay-Arts, et al.
European Journal of Medical Genetics|March 1, 2006
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literatureI Feenstra, D A Koolen, J Van der Pas, et al.
European Journal of Medical Genetics|July 11, 2006
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalitiesI Feenstra, J Fang, D A Koolen, et al.
Pageof 2