The clinical spectrum of complete FBN1 allele deletions von HILHORST-HOFSTEE, Yvonne, HAMEL, Ben Cj, MOLL, Henriette A, BREUNING, Martijn H, PALS, Gerard, VERHEIJ, Joke Bgm, RIJLAARSDAM, Marry Eb, MANCINI, Grazia Ms, COBBEN, Jan M, GIROTH, Cindy, RUIVENKAMP, Claudia Al, HANSSON, Kerstin Bm, TIMMERMANS, Janneke

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Pregnancy complications in singleton pregnancies with isolated fetal heart defects von van Velzen, Christine L., Türkeri, Freya, Pajkrt, Eva, Clur, Sally-Ann, Rijlaarsdam, Marry E.B., Bax, Caroline J., Hruda, Jaroslav, de Groot, Christianne J.M., Blom, Nico A., Haak, Monique C.

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Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects von Jansen, Fenna A. R., Hoffer, Mariette J. V., van Velzen, Christine L., Plati, Stephani Klingeman, Rijlaarsdam, Marry E. B., Clur, Sally-Ann B., Blom, Nico A., Pajkrt, Eva, Bhola, Shama L., Knegt, Alida C., de Boer, Marion A., Haak, Monique C.

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The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive family von Hilhorst-Hofstee, Yvonne, Rijlaarsdam, Marry EB, Scholte, Arthur JHA, Swart-van den Berg, Marietta, Versteegh, Michel IM, van der Schoot-van Velzen, Iris, Schäbitz, Hans-Joachim, Bijlsma, Emilia K, Baars, Marieke J, Kerstjens-Frederikse, Wilhelmina S, Giltay, Jacques C, Hamel, Ben C, Breuning, Martijn H, Pals, Gerard

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The clinical spectrum of complete allele deletions von Hilhorst-Hofstee, Yvonne, Hamel, Ben Jc, Verheij, Joke B.G.M., Rijlaarsdam, Marry Eb, Mancini, Grazia Ms, Cobben, Jan Maarten, Giroth, Cindy, Ruivenkamp, Claudia, Hansson, Kerstin B.M., Timmermans, Janneke, Moll, Henriette, Breuning, Martijn H., Pals, Gerard

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