Non‐coding variation in disorders of sex development von Baetens, D., Mendonça, B.B., Verdin, H., Cools, M., De Baere, E.

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Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series von Tack, L J W, Brachet, C, Beauloye, V, Heinrichs, C, Boros, E, De Waele, K, van der Straaten, S, Van Aken, S, Craen, M, Lemay, A, Rochtus, A, Casteels, K, Beckers, D, Mouraux, T, Logghe, K, Van Loocke, M, Massa, G, Van de Vijver, K, Syryn, H, Van De Velde, J, De Baere, E, Verdin, H, Cools, M

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Identification of novel disease gene for primary congenital glaucoma (PCG) through homozygosity mapping and next‐generation sequencing strategies in a large consanguineous pedigree... von VERDIN, H

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Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus von AlMoallem, Basamat, Bauwens, Miriam, Walraedt, Sophie, Delbeke, Patricia, De Zaeytijd, Julie, Kestelyn, Philippe, Meire, Françoise, Janssens, Sandra, van Cauwenbergh, Caroline, Verdin, Hannah, Hooghe, Sally, Kumar Thakur, Prasoon, Coppieters, Frauke, De Leeneer, Kim, Devriendt, Koenraad, Leroy, Bart P, De Baere, Elfride

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Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series von Tack, L.J.W, Brachet, C, Beauloye, V, Heinrichs, C, Boros, E, De Waele, K, van der Straaten, S, Van Aken, S, Craen, M, Lemay, A, Rochtus, A, Casteels, K, Beckers, D, Mouraux, T, Logghe, K, Van Loocke, M, Massa, G, van de Vijver, K, Syryn, H, Van De Velde, J, De Baere, E, Verdin, H, Cools, M

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Interleukin-12 regulates the production of Bacille Calmette-Guérin-induced interferon-gamma from human cells in a CD40-dependent manner von Méndez-Samperio, P, Ayala-Verdin, H E, Trejo-Echeverria, A

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Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II von Haghighi, Alireza, Verdin, Hannah, Haghighi-Kakhki, Hamidreza, Piri, Niloofar, Gohari, Nasrollah Saleh, De Baere, Elfride

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Novel and known FRMD7 mutations and copy number variation in Belgian patients with X‐linked idiopathic infantile nystagmus von ALMOALLEM, B, BAUWENS, M, WALRAEDT, S, DELBEKE, P, VERDIN, H, VAN CAUWENBERGH, C, DE LEENEER, K, HOOGHE, S, KESTELYN, P, AL‐OBEIDAN, S, DE ZAEYTIJD, J, LEROY, BP, DE BAERE, E

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Evaluation of Robenidine to Defaunate Pelibuey Lambs and the Production and Digestibility von Lopez Cama, J., Orozco-Her, J.R., Medina-Vil, J.H., Uribe-Gome, J.J., Verdin-San, H., Fuentes-He, V.O.

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Identification of novel disease gene for primary congenital glaucoma (PCG) through homozygosity mapping and next-generation sequencing von Verdin, H, De Baere, E, Kestelyn, P

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A. J. PODLECKI, The Life of Themistocles. A Critical Survey of the Literary and Archaeological Evidence. Montréal-London, McGill - Queen's University Press, 1975. XIV, 250 p. Pr. D... von Verdin, H

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S. HORNBLOWER, Thucydides. Baltimore, The Johns Hopkins University Press, 1987. IX, 230 pp von Verdin, H.

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Effect of cellulase on the digestibility of sodium hydroxide treated Tequilana agave bagasse von Paredes-Ibarra, F.J., Orozco-Hernández, J.R., Verdín-Sánchez, H., Montañez-Valdez, O.D., Alvarado-Loza, E., Fuentes Hernández, V.O.

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The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56 von Almoallem, B, Arno, G, De Zaeytijd, J, Verdin, H, Balikova, I, Casteels, I, de Ravel, T, Hull, S, Suzani, M, Destrée, A, Peng, M, Williams, D, Ainsworth, JR, Webster, AR, Leroy, BP, Moore, AT, De Baere, E

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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease von Van de Sompele, S, Smith, C, Karali, M, Corton, M, Van Schil, K, Peelman, F, Cherry, T, Rosseel, T, Verdin, H, Derolez, J, Van Laethem, T, Khan, KN, McKibbin, M, Toomes, C, Ali, M, Torella, A, Testa, F, Jimenez, B, Simonelli, F, De Zaeytijd, J, Van den Ende, J, Leroy, BP, Coppieters, F, Ayuso, C, Inglehearn, CF, Banfi, S, De Baere, E

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Regulation of interleukin-12 production in human cells stimulated with Mycobacterium bovis BCG von Méndez-Samperio, P, Trejo-Echeverria, A, Ayala-Verdin, H

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Correction to: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease von Van de Sompele, S, Smith, C, Karali, M, Corton, M, Van Schil, K, Peelman, F, Cherry, T, Rosseel, T, Verdin, H, Derolez, J, Van Laethem, T, Khan, KN, McKibbin, M, Toomes, C, Ali, M, Torella, A, Testa, F, Jimenez, B, Simonelli, F, De Zaeytijd, J, Van den Ende, J, Leroy, BP, Coppieters, F, Ayuso, C, Inglehearn, CF, Banfi, S, De Baere, E

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IDENTIFICATION OF NOVEL DISEASE GENE FOR PRIMARY CONGENITAL GLAUCOMA (PCG) THROUGH HOMOZYGOSITY MAPPING AND NEXT-GENERATION SEQUENCING : 2010 FRO PROJECTS von VERDIN, H, DE BAERE, E, KESTELYN, P

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S. HORNBLOWER, Thucydides. Baltimore, The Johns Hopkins University Press, 1987. IX, 230 pp von Verdin, H

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A restricted repertoire of de novo mutations in ITPR1 cause Gillespie Syndrome with evidence for dominant-negative effect von McEntagart, M, Williamson, KA, Rainger, JK, Wheeler, A, Seawright, A, De Baere, E, Verdin, H, Bergendahl, LT, Quigley, A, Rainger, J, Dixit, A, Sarkar, A, López Laso, E, Sanchez-Carpintero, R, Barrio, J, Bitoun, P, Prescott, T, Riise, R, McKee, S, Cook, J, McKie, L, Ceulemans, B, Meire, F, Temple, IK, Prieur, F, Williams, J, Clouston, P, Németh, AH, Banka, S, Bengani, H, Handley, M, Freyer, E, Ross, A, DDD Study, van Heyningen, V, Marsh, JA, Elmslie, F, FitzPatrick, DR

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