Raoul C M Hennekam
9PUBLICATIONS
40CO-AUTHORS
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Publications (9)
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|Feb 13, 2023
A Pellino-2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium-digital keloid dysplasia.Ileana Cristea, Hugo Abarca, Anne E Christensen Mellgren
|Nov 03, 2020
Genetic control of tumor development in malformation syndromes.Floor A M Postema, Jan C Oosterwijk, Raoul C Hennekam
|Apr 09, 2020
Primrose syndrome: Characterization of the phenotype in 42 patients.Daniela Melis, Daniel Carvalho, Tina Barbaro-Dieber
|Mar 21, 2020
Delineation of phenotypes and genotypes related to cohesin structural protein RAD21.Lianne C Krab, Iñigo Marcos-Alcalde, Melissa Assaf
|Aug 31, 2019
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.Muriel de La Dure-Molla, Benjamin Philippe Fournier, Maria Cristina Manzanares
|Jun 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.Suzanna G M Frints, Friederike Hennig, Roberto Colombo
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Frequent Collaborators
1 joint publications
Floor A M Postema
1 joint publications
Ariana Kariminejad
1 joint publications
Hassan Vahidnezhad
1 joint publications
Suzanna G M Frints
1 joint publications
Servi J C Stevens
1 joint publications
Merryn V E Macville
1 joint publications
Arthur S Lee
1 joint publications
Elizabeth C Engle
1 joint publications
Vera M Kalscheuer
1 joint publications
Muriel de La Dure-Molla
