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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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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Array-based DNA copy number analysis for mullerian anomalies von Santos, X.M, Bravo, J, Wang, X, Van den Veyver, I.B, Dietrich, J.E

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Genetic screening and testing in pregnancies conceived by in vitro fertilization (IVF) with preimplantation genetic screening (PGS) von Arian, S., Westerfield, L., Erfani, H., Nassef, S., Buffie, A., Gibbons, W.E., Van den Veyver, I.B.

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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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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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DNA methylation of the estrogen receptor alpha gene promoter in human granulosa cells von Kovanci, E., Amato, P., McKenzie, L.J., Sierra, R., Carson, S.A., Van Den Veyver, I.B.

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Characterization of a novel candidate gene in Xp22.3 with homology to Drosophila ms13 von Van den Veyver, I.B., Prakash, S., Franco, B., Zoghbi, H.Y.

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