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Nederlands Tijdschrift Voor Geneeskunde|January 23, 2014
[Introduction of next-generation sequencing in health care: what are the implications for physicians and patients?]Corrette Ploem, Wybo Dondorp, Guido de Wert, et al.
European Journal of Medical Genetics|March 25, 2019
Experts reflecting on the duty to recontact patients and research participants; why professionals should take the lead in developing guidelinesColin Mitchell, Corrette Ploem, Valesca Retèl, et al.
Developmental Medicine and Child Neurology|May 11, 2007
The Capacity Profile: a method to classify additional care needs in children with neurodevelopmental disabilitiesAnke Meester-Delver, Anita Beelen, Raoul Hennekam, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
MICRO syndrome: an entity distinct from COFS syndromeJohn M Graham, Raoul Hennekam, William B Dobyns, et al.
Developmental Medicine and Child Neurology|January 19, 2006
Predicting additional care in young children with neurodevelopmental disability: a systematic literature reviewAnke Meester-Delver, Anita Beelen, Raoul Hennekam, et al.
Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery|July 16, 2005
Follow-up of a girl with cleft lip and palate and multiple malformations: trisomy 20 mosaicismPetter Strømme, Carl Birger van der Hagen, Monika Haakonsen, et al.
American Journal of Medical Genetics. Part A|July 10, 2007
Autosomal recessive mental retardation syndrome with anterior maxillary protrusion and strabismus: MRAMS syndromeLina Basel-Vanagaite, Limor Rainshtein, Dov Inbar, et al.
BMC Medical Genetics|June 10, 2008
Variation in WNT7A is unlikely to be a cause of familial congenital talipes equinovarusGuoqing Liu, Julie Inglis, Amanda Cardy, et al.
European Thyroid Journal|July 17, 2023
The role of transducin β-like 1 X-linked receptor 1 (TBL1XR1) in thyroid hormone metabolism and action in miceYalan Hu, Kim Falize, A S Paul van Trotsenburg, et al.
European Journal of Cancer (Oxford, England : 1990)|March 12, 2013
Structural genome variations in individuals with childhood cancer and tumour predisposition syndromesSaskia Hopman, Johannes Merks, Hubertus Eussen, et al.
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