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B Van Der Zwaag

Showing results (1-10 of 9) with videos related to

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The Netherlands Journal of Medicine|March 11, 2015
Solving a cold case of haemolysis: back to the basicsR Bijleveld, J de Kok, B van der Zwaag, et al.
International Journal of Laboratory Hematology|May 11, 2017
Profound spherocytosis in adulthood: Acquired, hereditary or both?T J C Langeveld, A P van Rossum, B van der Zwaag, et al.
Neurology|February 25, 2005
The neuropathology of hereditary congenital facial palsy vs Möbius syndromeH T F M Verzijl, B van der Zwaag, M Lammens, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 30, 2017
[Genetic obesity: new diagnostic options]T I de Vries, S I M Alsters, L Kleinendorst, et al.
European Journal of Medical Genetics|January 11, 2020
Fraser syndrome without cryptophthalmos: Two casesS Boussion, S Lyonnet, B Van Der Zwaag, et al.
Journal of Medical Genetics|June 19, 2002
Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10B Van Der Zwaag, H T F M Verzijl, D Beltran-Valero De Bernabe, et al.
Leukemia|March 21, 2012
Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigreesA Buijs, M Poot, S van der Crabben, et al.
Obesity Surgery|October 26, 2019
Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid ObesityM I Cooiman, L Kleinendorst, E O Aarts, et al.
Molecular Psychiatry|March 24, 2010
A double hit implicates DIAPH3 as an autism risk geneJ A S Vorstman, E van Daalen, G R Jalali, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The Netherlands Journal of Medicine|March 11, 2015
Solving a cold case of haemolysis: back to the basicsR Bijleveld, J de Kok, B van der Zwaag, et al.
International Journal of Laboratory Hematology|May 11, 2017
Profound spherocytosis in adulthood: Acquired, hereditary or both?T J C Langeveld, A P van Rossum, B van der Zwaag, et al.
Neurology|February 25, 2005
The neuropathology of hereditary congenital facial palsy vs Möbius syndromeH T F M Verzijl, B van der Zwaag, M Lammens, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 30, 2017
[Genetic obesity: new diagnostic options]T I de Vries, S I M Alsters, L Kleinendorst, et al.
European Journal of Medical Genetics|January 11, 2020
Fraser syndrome without cryptophthalmos: Two casesS Boussion, S Lyonnet, B Van Der Zwaag, et al.
Journal of Medical Genetics|June 19, 2002
Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10B Van Der Zwaag, H T F M Verzijl, D Beltran-Valero De Bernabe, et al.
Leukemia|March 21, 2012
Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigreesA Buijs, M Poot, S van der Crabben, et al.
Obesity Surgery|October 26, 2019
Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid ObesityM I Cooiman, L Kleinendorst, E O Aarts, et al.
Molecular Psychiatry|March 24, 2010
A double hit implicates DIAPH3 as an autism risk geneJ A S Vorstman, E van Daalen, G R Jalali, et al.
Pageof 1