Further refinement of the candidate region for monosomy 9p syndrome von Faas, Brigitte H.W., de Leeuw, Nicole, Mieloo, Hanneke, Bruinenberg, Jos, de Vries, Bert B.A.

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Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies von NOWAKOWSKA, Beata A, DE LEEUW, Nicole, PFUNDT, Rolph, MIELOO, Hanneke, VAN ESSEN, Ton, DE VRIES, Bert Ba, GREEN, Andrew, REARDON, Willie, FRYNS, Jean-Pierre, VERMEESCH, Joris R, RUIVENKAMP, Claudia Al, SIKKEMA-RADDATZ, Birgit, CROLLA, John A, THOELEN, Reinhilde, KOOPMANS, Marije, DEN HOLLANDER, Nicolette, VAN HAERINGEN, Arie, VAN DER KEVIE-KERSEMAEKERS, Anne-Marie

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Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations: Noninvasive prenatal testing by two-channel SB... von Neveling, Kornelia, Tjwan Thung, Djie, Beulen, Lean, van Rens-Buijsman, Wendy, Gomes, Ingrid, van den Heuvel, Simone, Mieloo, Hanneke, Derks-Prinsen, Irma, Kater-Baats, Ellen, Faas, Brigitte H. W.

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Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations von Neveling, Kornelia, Tjwan Thung, Djie, Beulen, Lean, van Rens-Buijsman, Wendy, Gomes, Ingrid, van den Heuvel, Simone, Mieloo, Hanneke, Derks-Prinsen, Irma, Kater-Baats, Ellen, Faas, Brigitte H. W.

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Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome von Freriks, Kim, Timmers, Henri J.L.M, Netea-Maier, Romana T, Beerendonk, Catharina C.M, Otten, Barto J, van Alfen-van der Velden, Janiëlle A.E.M, Traas, Maaike A.F, Mieloo, Hanneke, van de Zande, Guillaume W.H.J.F.L, Hoefsloot, Lies H, Hermus, Ad R.M.M, Smeets, Dominique F.C.M

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Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature von Kleefstra, Tjitske, de Leeuw, Nicole, Wolf, Roy, Nillesen, Willy M., Schobers, Gaby, Mieloo, Hanneke, Willemsen, Marjolein, Perrotta, Concetta Simona, Poddighe, Pino J., Feenstra, Ilse, Draaisma, Jos, van Ravenswaaij-Arts, Conny M.A.

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Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies von Nowakowska, Beata, de Leeuw, Nicole, Ruivenkamp, Claudia Al, Sikkema-Raddatz, Birgit, Crolla, John A, Thoelen, Reinhilde, Koopmans, Marije, den Hollander, Nicolette, van Haeringen, Arie, van der Kevie-Kersemaekers, Anne-Marie, Pfundt, Rolph, Mieloo, Hanneke, van Essen, Ton, de Vries, Bert B.A, Green, Andrew, Reardon, Willie, Fryns, Jean-Pierre, Vermeesch, Joris

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Phenotypic Spectrum of 20 Novel Patients With Molecularly Defined Supernumerary Marker hromosomes 15 and a Review of the Literature von KLEEFSTRA, Tjitske, DE LEEUW, Nicole, DRAAISMA, Jos, VAN RAVENSWAAIJ-ARTS, Conny M. A, WOLF, Roy, NILLESEN, Willy M, SCHOBERS, Gabg, MIELOO, Hanneke, WILLEMSEN, Marjolein, PERROTTA, Concetta Simona, PODDIGHE, Pino J, FEENSTRA, Ilse

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Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features von Kleefstra, T, van de Zande, G, Merkx, G, Mieloo, H, Hoovers, J M, Smeets, D

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Identification of an unbalanced cryptic translocation between the chromosomes8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features von Kleefstra, Tjitske, van de Zande, Guillaume, Merkx, Gerard, Mieloo, Hanneke, Hoovers, Jan MN, Smeets, Dominique

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Further refinement of the candidate region for monosomy 9p syndrome von Faas, Brigitte H W, de Leeuw, Nicole, Mieloo, Hanneke, Bruinenberg, Jos, de Vries, Bert B A

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