Reply to Happle

由 Houge, Gunnar, Hennekam, Raoul C M
出版 2009

Body Integrity Identity Disorder

由 Blom, Rianne M., Hennekam, Raoul C., Denys, Damiaan
出版 2012

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

由 Kranendonk, Elcke J., Hennekam, Raoul C., Ploem, M. Corrette
發表在 Eur J Pediatr (2016)

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

由 Kranendonk, Elcke J, Hennekam, Raoul C, Ploem, Martine Corrette
發表在 Eur J Hum Genet (2017)

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

由 Kranendonk, Elcke J, Ploem, M Corrette, Hennekam, Raoul C M
發表在 Eur J Hum Genet (2016)

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

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

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

由 Cardy, Amanda H., Sharp, Linda, Torrance, Nicola, Hennekam, Raoul C., Miedzybrodzka, Zosia
出版 2011

The Face Signature of Fibrodysplasia Ossificans Progressiva

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

Rubinstein–Taybi syndrome (CREBBP, EP300)

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

Growth charts for children with Ellis–van Creveld syndrome

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

Face shape differs in phylogenetically related populations

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

Elements of Morphology: Standard Terminology for the External Genitalia

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

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

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

Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings

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

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

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

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

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

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

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

Benign and malignant tumors in Rubinstein–Taybi syndrome

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

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

由 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.
出版 2006

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

由 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
發表在 Clin Transl Allergy (2016)