Reply to Happle

par Houge, Gunnar, Hennekam, Raoul C M
Publié 2009

Body Integrity Identity Disorder

par Blom, Rianne M., Hennekam, Raoul C., Denys, Damiaan
Publié 2012

Paediatric biobanking: Dutch experts reflecting on appropriate legal standards for practice

par Kranendonk, Elcke J., Hennekam, Raoul C., Ploem, M. Corrette
Publié dans Eur J Pediatr (2016)

The Dutch legal approach regarding health care decisions involving minors in the NGS days

par Kranendonk, Elcke J, Hennekam, Raoul C, Ploem, Martine Corrette
Publié dans Eur J Hum Genet (2017)

Regulating biobanking with children's tissue: a legal analysis and the experts' view

par Kranendonk, Elcke J, Ploem, M Corrette, Hennekam, Raoul C M
Publié dans Eur J Hum Genet (2016)

Renal malformations associated with mutations of developmental genes: messages from the clinic

par Adalat, Shazia, Bockenhauer, Detlef, Ledermann, Sarah E., Hennekam, Raoul C., Woolf, Adrian S.
Publié 2010

Is There Evidence for Aetiologically Distinct Subgroups of Idiopathic Congenital Talipes Equinovarus? A Case-Only Study and Pedigree Analysis

par Cardy, Amanda H., Sharp, Linda, Torrance, Nicola, Hennekam, Raoul C., Miedzybrodzka, Zosia
Publié 2011

The Face Signature of Fibrodysplasia Ossificans Progressiva

par Hammond, Peter, Suttie, Michael, Hennekam, Raoul C., Allanson, Judith, Shore, Eileen M., Kaplan, Frederick S.
Publié 2012

Rubinstein–Taybi syndrome (CREBBP, EP300)

par van Belzen, Martine, Bartsch, Oliver, Lacombe, Didier, Peters, Dorien J M, Hennekam, Raoul C M
Publié 2011

Growth charts for children with Ellis–van Creveld syndrome

par Verbeek, Sabine, Eilers, Paul H. C., Lawrence, Kate, Hennekam, Raoul C. M., Versteegh, Florens G. A.
Publié 2010

Face shape differs in phylogenetically related populations

par Hopman, Saskia M J, Merks, Johannes H M, Suttie, Michael, Hennekam, Raoul C M, Hammond, Peter
Publié 2014

Elements of Morphology: Standard Terminology for the External Genitalia

par Hennekam, Raoul C.M., Allanson, Judith E., Biesecker, Leslie G., Carey, John C., Opitz, John M., Vilain, Eric
Publié dans Am J Med Genet A (2013)

Phenotype and natural history in 101 individuals with Pitt-Hopkins syndrome through an internet questionnaire system

par de Winter, Channa F., Baas, Melanie, Bijlsma, Emilia K., van Heukelingen, John, Routledge, Sue, Hennekam, Raoul C. M.
Publié dans Orphanet J Rare Dis (2016)

Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings

par Chen, Bee Chin, Mohd Rawi, Rowani, Meinsma, Rutger, Meijer, Judith, Hennekam, Raoul C.M., van Kuilenburg, André B.P.
Publié dans Mol Syndromol (2014)

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

par Bartholdi, Deborah, Roelfsema, Jeroen H, Papadia, Francesco, Breuning, Martijn H, Niedrist, Dunja, Hennekam, Raoul C, Schinzel, Albert, Peters, Dorien J M
Publié 2007

Genetic susceptibility for cow’s milk allergy in Dutch children: the start of the allergic march?

par Henneman, Peter, Petrus, Nicole C. M., Venema, Andrea, van Sinderen, Femke, van der Lip, Karin, Hennekam, Raoul C., Mannens, Marcel, Sprikkelman, Aline B.
Publié dans Clin Transl Allergy (2016)

Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1

par van Kuilenburg, André B. P., Meijer, Judith, Meinsma, Rutger, Pérez-Dueñas, Belén, Alders, Marielle, Bhuiyan, Zahurul A., Artuch, Rafael, Hennekam, Raoul C. M.
Publié dans JIMD Rep (2018)

Benign and malignant tumors in Rubinstein–Taybi syndrome

par Boot, Max V., van Belzen, Martine J., Overbeek, Lucy I., Hijmering, Nathalie, Mendeville, Matias, Waisfisz, Quinten, Wesseling, Pieter, Hennekam, Raoul C., de Jong, Daphne
Publié dans Am J Med Genet A (2018)

Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase

par Lesnik Oberstein, Saskia A. J., Kriek, Marjolein, White, Stefan J., Kalf, Margot E., Szuhai, Karoly, den Dunnen, Johan T., Breuning, Martijn H., Hennekam, Raoul C. M.
Publié 2006

Cow’s milk allergy in Dutch children: an epigenetic pilot survey

par Petrus, Nicole C. M., Henneman, Peter, Venema, Andrea, Mul, Adri, van Sinderen, Femke, Haagmans, Martin, Mook, Olaf, Hennekam, Raoul C., Sprikkelman, Aline B., Mannens, Marcel
Publié dans Clin Transl Allergy (2016)