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Peptides|January 1, 1995
Neuropeptide Y inhibits Ca2+ oscillations, cyclic AMP, and secretion in melanotrope cells of Xenopus laevis via a Y1 receptorW J Scheenen, H G Yntema, P H Willems, et al.Clinical Neuropathology|November 16, 2010
Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosisD Wallon, L Guyant-Maréchal, A Laquerrière, et al.European Journal of Medical Genetics|October 5, 2014
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disabilityJ M Cobben, M M Weiss, F S van Dijk, et al.Molecular Syndromology|July 26, 2013
Noonan syndrome: comparing mutation-positive with mutation-negative dutch patientsE A Croonen, W Nillesen, C Schrander, et al.Case Reports in Radiology|August 1, 2012
Occult Breast Cancer due to Multiple Calcified Hamartomas in a Patient with Cowden SyndromeE B Gómez García, M B I Lobbes, K van de Vijver, et al.Clinical Genetics|June 26, 2002
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.European Journal of Pediatrics|June 2, 2019
The etiological evaluation of sensorineural hearing loss in childrenE A van Beeck Calkoen, M S D Engel, J M van de Kamp, et al.Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.Journal of the Association for Research in Otolaryngology : JARO|April 23, 2025
Cochlear Implantation Outcomes in Genotyped Subjects with Sensorineural Hearing LossM L A Fehrmann, L Haer-Wigman, H Kremer, et al.Pageof 3