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Hennekam, Raoul
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1

The role of transducin β-like 1 X-linked receptor 1 (TBL1XR..:

Hu, Yalan ; Falize, Kim ; van Trotsenburg, A S Paul...
European Thyroid Journal.  12 (2023)  5 - p. , 2023
Link: https://doi.org/10.1530/..
 
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2

An animal model for Pierpont syndrome: a mouse bearing the ..:

Hu, Yalan ; Lauffer, Peter ; Stewart, Michelle...
Human Molecular Genetics.  31 (2022)  17 - p. 2951-2963 , 2022
Link: https://doi.org/10.1093/..
 
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3

Experts reflecting on the duty to recontact patients and re..:

Mitchell, Colin ; Ploem, Corrette ; Retèl, Valesca..
European Journal of Medical Genetics.  63 (2020)  2 - p. 103642 , 2020
Link: https://doi.org/10.1016/..
 
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4

Revisiting Wilms tumour surveillance in Beckwith–Wiedemann ..:

Brioude, Frédéric ; Hennekam, Raoul ; Bliek, Jet...
European Journal of Human Genetics.  26 (2018)  4 - p. 471-472 , 2018
Link: https://doi.org/10.1038/..
 
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5

Self-injurious behavior:

Huisman, Sylvia ; Mulder, Paul ; Kuijk, Janneke...
Neuroscience & Biobehavioral Reviews.  84 (2018)  - p. 483-491 , 2018
Link: https://doi.org/10.1016/..
 
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6

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Opht..:

Rainger, Joe ; van Beusekom, Ellen ; Ramsay, Jacqueline K....
PLOS Genetics.  14 (2018)  12 - p. e1007866 , 2018
Link: https://doi.org/10.1371/..
 
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7

Variants in members of the cadherin–catenin complex, CDH1 a..:

Kievit, Anneke ; Tessadori, Federico ; Douben, Hannie...
European Journal of Human Genetics.  26 (2018)  2 - p. 210-219 , 2018
Link: https://doi.org/10.1038/..
 
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8

Exploring the potential duty of care in clinical genomics u..:

Mitchell, Colin ; Ploem, Corrette ; Chico, Victoria...
Medical Law International.  17 (2017)  3 - p. 158-182 , 2017
Link: https://doi.org/10.1177/..
 
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9

Analysis of mutations within the intron20 splice donor site..:

Dauwerse, Johannes G ; van Belzen, Martine ; van Haeringen, Arie...
European Journal of Human Genetics.  24 (2016)  11 - p. 1639-1643 , 2016
Link: https://doi.org/10.1038/..
 
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10

Syndrome disintegration: Exome sequencing reveals that Fitz..:

Armour, Christine M. ; Smith, Amanda ; Hartley, Taila...
American Journal of Medical Genetics Part A.  170 (2016)  7 - p. 1820-1825 , 2016
Link: https://doi.org/10.1002/..
 
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11

Loss-of-function HDAC8 mutations cause a phenotypic spectru..:

Kaiser, Frank J. ; Ansari, Morad ; Braunholz, Diana...
Human Molecular Genetics.  23 (2014)  11 - p. 2888-2900 , 2014
Link: https://doi.org/10.1093/..
 
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12

Opposite effects on facial morphology due to gene dosage se..:

Hammond, Peter ; McKee, Shane ; Suttie, Michael...
Human Genetics.  133 (2014)  9 - p. 1117-1125 , 2014
Link: https://doi.org/10.1007/..
 
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13

Structural genome variations in individuals with childhood ..:

Hopman, Saskia ; Merks, Johannes ; Eussen, Hubertus...
European Journal of Cancer.  49 (2013)  9 - p. 2170-2178 , 2013
Link: https://doi.org/10.1016/..
 
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14

Diagnostic outcomes of 27 children referred by pediatrician..:

Abdelmalik, Nadia ; van Haelst, Mieke ; Mancini, Grazia...
American Journal of Medical Genetics Part A.  161 (2013)  2 - p. 254-260 , 2013
Link: https://doi.org/10.1002/..
 
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15

Atypical face shape and genomic structural variants in epil..:

Chinthapalli, Krishna ; Bartolini, Emanuele ; Novy, Jan...
Brain.  135 (2012)  10 - p. 3101-3114 , 2012
Link: https://doi.org/10.1093/..
 
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