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Mieke M van Haelst

Showing results (1-10 of 139) with videos related to

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JAMA Neurology|December 4, 2023
Mirror Hand Movements Caused by a Deletion of the DCC GeneLotte Kleinendorst, Mieke M van Haelst
Nederlands Tijdschrift Voor Geneeskunde|April 5, 2019
[A girl with 16p11.2 deletion syndrome]Lotte Kleinendorst, Marthe Sno, Mieke M van Haelst
The New England Journal of Medicine|July 20, 2022
Obesity-Associated GNAS Mutations and the Melanocortin PathwayLotte Kleinendorst, Elles Boon, Mieke M van Haelst
Journal of Pediatric Genetics|September 15, 2016
Ciliary disturbances in syndromal and non-syndromal obesityTamar I de Vries, Mieke M van Haelst
BMJ Case Reports|July 13, 2021
Young adult with Cantú syndrome: dealing with a rare genetic skin disorderHelen I Roessler, Gijs van Haaften, Mieke M van Haelst
Nederlands Tijdschrift Voor Geneeskunde|September 4, 2024
[Direct-to-consumer genetic tests in the Netherlands: impact on consumers and clinical practice]Danny Bruins, Suzanne M Onstwedder, Mieke M van Haelst, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Fraser syndrome: a clinical study of 59 cases and evaluation of diagnostic criteriaMieke M van Haelst, Peter J Scambler, , et al.
Experientia Supplementum (2012)|October 8, 2019
Genetics of ObesityLotte Kleinendorst, Mieke M van Haelst, Erica L T van den Akker
BMJ Case Reports|September 28, 2017
Young girl with severe early-onset obesity and hyperphagiaLotte Kleinendorst, Mieke M van Haelst, Erica L T van den Akker
European Journal of Human Genetics : EJHG|August 30, 2022
"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndromeLynne Rumping, Raoul C M Hennekam, Mariëlle Alders, et al.
Pageof 14

Showing results (1-10 of 139) with videos related to

Sort By:
Pageof 14
JAMA Neurology|December 4, 2023
Mirror Hand Movements Caused by a Deletion of the DCC GeneLotte Kleinendorst, Mieke M van Haelst
Nederlands Tijdschrift Voor Geneeskunde|April 5, 2019
[A girl with 16p11.2 deletion syndrome]Lotte Kleinendorst, Marthe Sno, Mieke M van Haelst
The New England Journal of Medicine|July 20, 2022
Obesity-Associated GNAS Mutations and the Melanocortin PathwayLotte Kleinendorst, Elles Boon, Mieke M van Haelst
Journal of Pediatric Genetics|September 15, 2016
Ciliary disturbances in syndromal and non-syndromal obesityTamar I de Vries, Mieke M van Haelst
BMJ Case Reports|July 13, 2021
Young adult with Cantú syndrome: dealing with a rare genetic skin disorderHelen I Roessler, Gijs van Haaften, Mieke M van Haelst
Nederlands Tijdschrift Voor Geneeskunde|September 4, 2024
[Direct-to-consumer genetic tests in the Netherlands: impact on consumers and clinical practice]Danny Bruins, Suzanne M Onstwedder, Mieke M van Haelst, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Fraser syndrome: a clinical study of 59 cases and evaluation of diagnostic criteriaMieke M van Haelst, Peter J Scambler, , et al.
Experientia Supplementum (2012)|October 8, 2019
Genetics of ObesityLotte Kleinendorst, Mieke M van Haelst, Erica L T van den Akker
BMJ Case Reports|September 28, 2017
Young girl with severe early-onset obesity and hyperphagiaLotte Kleinendorst, Mieke M van Haelst, Erica L T van den Akker
European Journal of Human Genetics : EJHG|August 30, 2022
"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndromeLynne Rumping, Raoul C M Hennekam, Mariëlle Alders, et al.
Pageof 14