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Martin Poot

Showing results (71-80 of 100) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 23, 2003
Zoledronic acid exhibits inhibitory effects on osteoblastic and osteolytic metastases of prostate cancerEva Corey, Lisha G Brown, Janna E Quinn, et al.
Aging Cell|July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processesAnna Maierhofer, Julia Flunkert, Junko Oshima, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and reviewWinnie Courtens, Wim Wuyts, Martin Poot, et al.
European Journal of Medical Genetics|April 14, 2009
Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the NetherlandsRon Hochstenbach, Ellen van Binsbergen, John Engelen, et al.
European Journal of Medical Genetics|October 13, 2007
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qterMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
Clinical Dysmorphology|April 30, 2011
Chromosomal abnormalities resembling Joubert syndrome: two cases illustrating the diagnostic pitfallsHester Y Kroes, Ron Hochstenbach, Rutger A J Nievelstein, et al.
Journal of Autism and Developmental Disorders|August 13, 2008
A novel 6.14 Mb duplication of chromosome 8p21 in a patient with autism and self mutilationHeval M Ozgen, Wouter G Staal, John C Barber, et al.
Journal of Child Neurology|September 29, 2011
Copy number variations in patients with electrical status epilepticus in sleepSietske H G Kevelam, Floor E Jansen, Ellen van Binsbergen, et al.
European Journal of Medical Genetics|September 7, 2011
A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12Oliver Bartsch, Detlev Schindler, Vera Beyer, et al.
Journal of the Neurological Sciences|June 5, 2007
Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathyMarijke Eurelings, Henk M Lokhorst, Nicolette C Notermans, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 23, 2003
Zoledronic acid exhibits inhibitory effects on osteoblastic and osteolytic metastases of prostate cancerEva Corey, Lisha G Brown, Janna E Quinn, et al.
Aging Cell|July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processesAnna Maierhofer, Julia Flunkert, Junko Oshima, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and reviewWinnie Courtens, Wim Wuyts, Martin Poot, et al.
European Journal of Medical Genetics|April 14, 2009
Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the NetherlandsRon Hochstenbach, Ellen van Binsbergen, John Engelen, et al.
European Journal of Medical Genetics|October 13, 2007
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qterMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
Clinical Dysmorphology|April 30, 2011
Chromosomal abnormalities resembling Joubert syndrome: two cases illustrating the diagnostic pitfallsHester Y Kroes, Ron Hochstenbach, Rutger A J Nievelstein, et al.
Journal of Autism and Developmental Disorders|August 13, 2008
A novel 6.14 Mb duplication of chromosome 8p21 in a patient with autism and self mutilationHeval M Ozgen, Wouter G Staal, John C Barber, et al.
Journal of Child Neurology|September 29, 2011
Copy number variations in patients with electrical status epilepticus in sleepSietske H G Kevelam, Floor E Jansen, Ellen van Binsbergen, et al.
European Journal of Medical Genetics|September 7, 2011
A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12Oliver Bartsch, Detlev Schindler, Vera Beyer, et al.
Journal of the Neurological Sciences|June 5, 2007
Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathyMarijke Eurelings, Henk M Lokhorst, Nicolette C Notermans, et al.
Pageof 10