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ir. O.P.P. van den Briels

ir. O.P.P. van den Briels

Assistant Professor - medical

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Research Output (86)

Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome:Clinical aspects

Hennekam R. C.M., Tilanus M., Hamel B. C.J., Voshart-van Heeren H., Mariman E. C.M., Van Beersum S. E.C., Van den Boogaard M. J.H., Breuning M. H. 1 Jan 1993, In: American Journal of Human Genetics. 52 , p. 255-262 8 p.

A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation

Van Den Boogaard M. J.H., De Pater J., Hennekam R. C.M. 5 Nov 1991, In: Genetic Counseling. 2 , p. 83-91 9 p.

A cephalometric study in Rubinstein-Taybi syndrome

Hennekam R. C M, Van Den Boogaard M. J., Van Doorne J. M. 1 Jan 1991, In: Journal of Craniofacial Genetics and Developmental Biology. 11 , p. 33-40 8 p.

Metacarpophalangeal pattern profile analysis in Rubinstein-Taybi syndrome

Hennekam R. C M, Van den Boogaard M. J., Dijkstra P. F., Van de Kamp J. J P 25 Sep 1990, In: American Journal of Medical Genetics. p. 48-50 3 p.

Rubinstein-Taybi syndrome in The Netherlands

Hennekam R. C.M., Van den Boogaard M. J., Sibbles B. J., Van Spijker H. G. 25 Sep 1990, In: American Journal of Medical Genetics. p. 17-29 13 p.

Autosomal dominant craniosynostosis of the sutura metopica

Hennekam Raoul C.M., van den Boogaard Marie‐Jose ‐J 1 Jan 1990, In: Clinical Genetics. 38 , p. 374-377 4 p.

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