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Clinical Genetics|November 1, 1990
Autosomal dominant craniosynostosis of the sutura metopicaR C Hennekam, M J Van den BoogaardGenetic Counseling (Geneva, Switzerland)|January 1, 1991
A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocationM J Van den Boogaard, J De Pater, R C HennekamJournal of Craniofacial Genetics and Developmental Biology|January 1, 1991
A cephalometric study in Rubinstein-Taybi syndromeR C Hennekam, M J Van den Boogaard, J M Van DoorneAmerican Journal of Medical Genetics. Supplement|January 1, 1990
Rubinstein-Taybi syndrome in The NetherlandsR C Hennekam, M J Van Den Boogaard, B J Sibbles, et al.American Journal of Medical Genetics. Supplement|January 1, 1990
Metacarpophalangeal pattern profile analysis in Rubinstein-Taybi syndromeR C Hennekam, M J Van Den Boogaard, P F Dijkstra, et al.Human Genetics|June 1, 1993
Identification of two new nucleotide mutations (HPRTUtrecht and HPRTMadrid) in exon 3 of the human hypoxanthine-guanine phosphoribosyltransferase (HPRT) geneA G Bouwens-Rombouts, M J van den Boogaard, J G Puig, et al.American Journal of Human Genetics|February 1, 1993
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspectsR C Hennekam, M Tilanus, B C Hamel, et al.Clinical Dysmorphology|October 1, 1993
The Peters'-Plus syndrome: description of 16 patients and review of the literatureR C Hennekam, M J Van Schooneveld, H H Ardinger, et al.Annals of Neurology|September 1, 1995
Genotype-phenotype correlation in adult-onset acid maltase deficiencyJ H Wokke, M G Ausems, M J van den Boogaard, et al.Clinical Genetics|October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disordersH M Ozgen, E van Daalen, P F Bolton, et al.Pageof 2