A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles von Kou, Y.C., Shao, L., Peng, H.H., Rosetta, R., del Gaudio, D., Wagner, A.F., Al-Hussaini, T.K., Van den Veyver, I.B.

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Implication of chromosomal microarray analysis prior to in‐utero repair of fetal open neural tube defect von Zemet, R., Krispin, E., Johnson, R. M., Kumar, N. R., Westerfield, L. E., Stover, S., Mann, D. G., Castillo, J., Castillo, H. A., Nassr, A. A., Sanz Cortes, M., Donepudi, R., Espinoza, J., Whitehead, W. E., Belfort, M. A., Shamshirsaz, A. A., Van den Veyver, I. B.

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Rett syndrome is caused by mutations in X-linked MECP2 , encoding methyl-CpG-binding protein 2 von Zoghbi, Huda Y, Amir, Ruthie E, Van den Veyver, Ignatia B, Wan, Mimi, Tran, Charles Q, Francke, Uta

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No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility von Aghajanova, L., Mahadevan, S., Altmäe, S., Stavreus-Evers, A., Regan, L., Sebire, N., Dixon, P., Fisher, R.A., Van den Veyver, I.B.

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The Product of the Imprinted Gene IPL Marks Human Villous Cytotrophoblast and is Lost in Complete Hydatidiform Mole von Saxena, A., Frank, D., Panichkul, P., Van den Veyver, I.B., Tycko, B., Thaker, H.

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Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring von Van den Veyver, I.B., Al-Hussaini, T.K.

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Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders? von van den Veyver, I.B.

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Recurrent pregnancy loss due to familial and non-familial habitual molar pregnancy von Al-Hussaini, T.K, Abd El Aal, D.M, Van den Veyver, I.B

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Skewed X Inactivation in X-Linked Disorders von Van den Veyver, Ignatia B.

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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome von Amir, R E, Fang, P, Yu, Z, Glaze, D G, Percy, A K, Zoghbi, H Y, Roa, B B, Van den Veyver, I B

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Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes von Amir, Ruthie E., Van Den Veyver, Ignatia B., Schultz, Rebecca, Malicki, Denise M., Tran, Charles Q., Dahle, E. J., Philippi, Anne, Timar, László, Percy, Alan K., Motil, Kathleen J., Lichtarge, Olivier, O'Brian Smith, E., Glaze, Daniel G., Zoghbi, Huda Y.

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Tooth Enamel Defects in Mice with a Deletion at the Arhgap6/AmelX Locus von Prakash, S. K., Gibson, C. W., Wright, J. T., Boyd, C., Cormier, T., Sierra, R., Li, Y., Abrams, W. R., Aragon, M. A., Yuan, Z. A., van den Veyver, I. B.

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Methyl-CpG-binding protein 2 mutations in Rett syndrome von Van den Veyver, Ignatia B, Zoghbi, Huda Y

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Terminal Osseous Dysplasia with Pigmentary Defects Maps to Human Chromosome Xq27.3-Xqter von Zhang, Wenzheng, Amir, Ruthie, Stockton, David W., Van den Veyver, Ignatia B., Bacino, Carlos A., Zoghbi, Huda Y.

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Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification von Kristjansson, Kristleifur, Chong, Samuel S, Van den Veyver, Ignatia B, Subramanian, Stephanie, Snabes, Michael C, Hughes, Mark R

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Characterization of a Novel Chromo Domain Gene in Xp22.3 with Homology to Drosophila msl-3 von Prakash, Siddharth K., Van den Veyver, Ignatia B., Franco, Brunella, Volta, Manuela, Ballabio, Andrea, Zoghbi, Huda Y.

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Characterization and Physical Mapping in Human and Mouse of a Novel RING Finger Gene in Xp22 von Van den Veyver, Ignatia B., Cormier, Trena A., Jurecic, Vesna, Baldini, Antonio, Zoghbi, Huda Y.

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Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome von Van den Veyver, Ignatia B., Zoghbi, Huda Y.

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Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy von Amir, Ruthie E, Sutton, V Reid, Van den Veyver, Ignatia B

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Genetic effects of methylation diets von VAN DEN VEYVER, Ignatia B

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