Pulmonary Fibrosis and a TERT Founder Mutation With a Latency Period of 300 Years von van der Vis, Joanne J., van der Smagt, Jasper J., Hennekam, Frederic A.M., Grutters, Jan C., van Moorsel, Coline H.M.

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Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms von Bakker, Mark K, Cobyte, Suze, Hennekam, Frederic A M, Rinkel, Gabriel J E, Veldink, Jan H, Ruigrok, Ynte M

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Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms von Bakker, Mark K, Cobyte, Suze, Hennekam, Frederic A.M, Rinkel, Gabriel J.E, Veldink, Jan H, Ruigrok, Ynte M

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A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene von Mul, Karlien, Schouten, Meyke I., van der Looij, Erica, Dooijes, Dennis, Hennekam, Frederic A.M., Notermans, Nicolette C., Praamstra, Peter, van Gaalen, Judith, Kamsteeg, Erik-Jan, Verbeek, Nienke E., van de Warrenburg, Bart P.C.

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Familial cutaneous cylindromas: Investigations in five generations of a family von Gerretsen, Anton L, Beemer, Frits A, Deenstra, Wilco, Hennekam, Frederic A.M, van Vloten, Willem A

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Angelman syndrome in an inbred family von BEUTEN, J, HENNEKAM, R. C. M, VAN ROY, B, MANGELSCHOTS, K, SUTCLIFFE, J. S, HALLEY, D. J. J, HENNEKAM, F. A. M, BEAUDET, A. L, WILLEMS, P. J

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