Showing results (1-10 of 40) with videos related to
Sort By:
Pageof 4
Nederlands Tijdschrift Voor Geneeskunde|April 5, 2019
[A girl with 16p11.2 deletion syndrome]Lotte Kleinendorst, Marthe Sno, Mieke M van HaelstExperientia Supplementum (2012)|October 8, 2019
Genetics of ObesityLotte Kleinendorst, Mieke M van Haelst, Erica L T van den AkkerBMJ Case Reports|September 28, 2017
Young girl with severe early-onset obesity and hyperphagiaLotte Kleinendorst, Mieke M van Haelst, Erica L T van den AkkerEuropean Journal of Human Genetics : EJHG|May 17, 2020
Who ever heard of 16p11.2 deletion syndrome? Parents' perspectives on a susceptibility copy number variation syndromeLotte Kleinendorst, Lieke M van den Heuvel, Lidewij Henneman, et al.Obesity Facts|July 2, 2023
The Narrative of a Patient with Leptin Receptor Deficiency: Personalized Medicine for a Rare Genetic Obesity DisorderMila S Welling, Lotte Kleinendorst, Mieke M van Haelst, et al.American Journal of Medical Genetics. Part A|September 22, 2018
The role of obesity in the fatal outcome of Schaaf-Yang syndrome: Early onset morbid obesity in a patient with a MAGEL2 mutationLotte Kleinendorst, Graciela Pi Castán, Alfonso Caro-Llopis, et al.European Journal of Medical Genetics|July 28, 2024
Phenotypic spectrum in Weiss-Kruszka syndrome caused by ZNF462 variants: Three new patients and literature reviewLiselot van der Laan, Lotte Kleinendorst, Johanna M van Hagen, et al.American Journal of Medical Genetics. Part A|January 19, 2026
The Voice of Cantú: Lower Voice Pitch Is a New Phenotypic Feature of Cantú SyndromeLotte Kleinendorst, Melanie N S Molegraaf, Dorothy K Grange, et al.Molecular Genetics & Genomic Medicine|May 6, 2019
Genetic analysis in the bariatric clinic; impact of a PTEN gene mutationMellody I Cooiman, Lotte Kleinendorst, Bert van der Zwaag, et al.European Journal of Human Genetics : EJHG|March 8, 2020
Second case of Bardet-Biedl syndrome caused by biallelic variants in IFT74Lotte Kleinendorst, Sanne I M Alsters, Ozair Abawi, et al.Pageof 4