Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives von Verhagen, Judith M.A., Kempers, Marlies, Cozijnsen, Luc, Bouma, Berto J., Duijnhouwer, Anthonie L., Post, Jan G., Hilhorst-Hofstee, Yvonne, Bekkers, Sebastiaan C.A.M., Kerstjens-Frederikse, Wilhelmina S., van Brakel, Thomas J., Lambermon, Eric, Wessels, Marja W., Loeys, Bart L., Roos-Hesselink, Jolien W., van de Laar, Ingrid M.B.H.

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Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives von Verhagen, Judith M.A, Kempers, Marlies, Cozijnsen, Luc, Bouma, Berto J, Duijnhouwer, Anthonie L, Post, Jan G, Hilhorst-Hofstee, Yvonne, Bekkers, Sebastiaan C.A.M, Kerstjens-Frederikse, Wilhelmina S, van Brakel, Thomas J, Lambermon, Eric, Wessels, Marja W, Loeys, Bart L, Roos-Hesselink, Jolien W, van de Laar, Ingrid M.B.H, National Working Group on BAV & TAA

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The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK von BRUNNER, H. G, VAN BENNEKOM, C. A, LAMBERMON, E. M. M, LIAN ŒI, T, CREMERS, C. W. R. J, WIERINGA, B, ROPERS, H.-H

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Localization of the gene for X-linked Alport's syndrome von Brunner, Han, Schröder, Cock, van Bennekom, Cor, Lambermon, Eric, Tuerlings, Joep, Menzel, Daria, Olbing, Hermann, Monnens, Leo, Wieringa, Berend, Ropers, Hans-Hilger

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Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q von Friedrich, U, Brunner, H, Smeets, D, Lambermon, E, Ropers, H H

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