Reply to Happle

por Houge, Gunnar, Hennekam, Raoul C M
Publicado 2009

Body Integrity Identity Disorder

por Blom, Rianne M., Hennekam, Raoul C., Denys, Damiaan
Publicado 2012

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

por Kranendonk, Elcke J., Hennekam, Raoul C., Ploem, M. Corrette
Publicado en Eur J Pediatr (2016)

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

por Kranendonk, Elcke J, Hennekam, Raoul C, Ploem, Martine Corrette
Publicado en Eur J Hum Genet (2017)

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

por Kranendonk, Elcke J, Ploem, M Corrette, Hennekam, Raoul C M
Publicado en Eur J Hum Genet (2016)

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

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

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

por Cardy, Amanda H., Sharp, Linda, Torrance, Nicola, Hennekam, Raoul C., Miedzybrodzka, Zosia
Publicado 2011

The Face Signature of Fibrodysplasia Ossificans Progressiva

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

Rubinstein–Taybi syndrome (CREBBP, EP300)

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

Growth charts for children with Ellis–van Creveld syndrome

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

Face shape differs in phylogenetically related populations

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

Elements of Morphology: Standard Terminology for the External Genitalia

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

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

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

Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings

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

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

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

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

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

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

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

Benign and malignant tumors in Rubinstein–Taybi syndrome

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

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

por 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.
Publicado 2006

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

por 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
Publicado en Clin Transl Allergy (2016)