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Cecilie F Rustad

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Hereditary Cancer in Clinical Practice|March 13, 2010
Germline PTEN mutations are rare and highly penetrantCecilie F Rustad, Merete Bjørnslett, Ketil R Heimdal, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 9, 2008
[A newborn infant with hyperventilation]Rolf Lindemann, Mia C Myhre, Mari Bakken, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 2020
Gene panel testingIda W Sørensen, Trine Prescott, Cecilie F Rustad, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 13, 2022
A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 2, 2022
Correction: A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
American Journal of Medical Genetics. Part A|August 12, 2022
Phenotypic expansion of ARSK-related mucopolysaccharidosisCecilie F Rustad, Trine E Prescott, Else Merckoll, et al.
American Journal of Medical Genetics. Part A|May 12, 2021
Positive response to imatinib in PDGFRB-related Kosaki overgrowth syndromeCecilie F Rustad, Kristian Tveten, Trine E Prescott, et al.
Clinical Dysmorphology|November 12, 2025
Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overviewTitas Gladkauskas, Ileana Cristea, Roya Mehrasa, et al.
Cold Spring Harbor Molecular Case Studies|October 7, 2021
Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum featuresSiren Berland, Cecilie F Rustad, Mariann H L Bentsen, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddlerCecilie F Rustad, Hilde M Dahl, Naomi L Bowers, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

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Pageof 4
Hereditary Cancer in Clinical Practice|March 13, 2010
Germline PTEN mutations are rare and highly penetrantCecilie F Rustad, Merete Bjørnslett, Ketil R Heimdal, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 9, 2008
[A newborn infant with hyperventilation]Rolf Lindemann, Mia C Myhre, Mari Bakken, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 2020
Gene panel testingIda W Sørensen, Trine Prescott, Cecilie F Rustad, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 13, 2022
A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 2, 2022
Correction: A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
American Journal of Medical Genetics. Part A|August 12, 2022
Phenotypic expansion of ARSK-related mucopolysaccharidosisCecilie F Rustad, Trine E Prescott, Else Merckoll, et al.
American Journal of Medical Genetics. Part A|May 12, 2021
Positive response to imatinib in PDGFRB-related Kosaki overgrowth syndromeCecilie F Rustad, Kristian Tveten, Trine E Prescott, et al.
Clinical Dysmorphology|November 12, 2025
Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overviewTitas Gladkauskas, Ileana Cristea, Roya Mehrasa, et al.
Cold Spring Harbor Molecular Case Studies|October 7, 2021
Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum featuresSiren Berland, Cecilie F Rustad, Mariann H L Bentsen, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddlerCecilie F Rustad, Hilde M Dahl, Naomi L Bowers, et al.
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