Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations von Di Donato, N, Rump, A, Koenig, R, Der Kaloustian, V M, Halal, F, Sonntag, K, Krause, C, Hackmann, K, Hahn, G, Schrock, E, Verloes, A

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Molecular Analysis of Collagen XVIII Reveals Novel Mutations, Presence of a Third Isoform, and Possible Genetic Heterogeneity in Knobloch Syndrome von Suzuki, O.T., Sertié, A.L., Der Kaloustian, V.M., Kok, F., Carpenter, M., Murray, J., Czeizel, A.E., Kliemann, S.E., Rosemberg, S., Monteiro, M., Olsen, B.R., Passos-Bueno, M.R.

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Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome von KOGAN, C. S, BERTONE, A, CORNISH, K, BOUTET, I, DER KALOUSTIAN, V. M, ANDERMANN, E, FAUBERT, J, CHAUDHURI, A

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Positional cloning of the gene for Nijmegen breakage syndrome von Komatsu, Kenshi, Matsuura, Shinya, Tauchi, Hiroshi, Nakamura, Asako, Kondo, Noriko, Sakamoto, Shuichi, Endo, Satoru, Smeets, Dominique, Solder, Brigitte, Belohradsky, Bernd H, Der Kaloustian, Vazken M, Oshimura, Mitsuo, Isomura, Minoru, Nakamura, Yusuke

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Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations von Di Donato, N, Rump, A, Koenig, R, Der Kaloustian, V M, Halal, F, Sonntag, K, Krause, C, Hackmann, K, Hahn, G, Schrock, E, Verloes, A

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Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome von Diaz-Meyer, N, Day, C D, Khatod, K, Maher, E R, Cooper, W, Reik, W, Junien, C, Graham, G, Algar, E, Der Kaloustian, V M, Higgins, M J

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Stable non-Robertsonian dicentric chromosomes: four new cases and a review von LEMYRE, EMMANUELLE, KALOUSTIAN, VAZKEN M DER, DUNCAN, ALESSANDRA M V

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Nijmegen breakage syndrome von The, I

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No mental retardation in a man with 40% abnormal methylation at the FMR-1 locus and transmission of sperm cell mutations as premutations von Rousseau, François, Robb, Laura J., Rouillard, Patricia, Kaloustian, Vazken M. Der

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The Gene Responsible for Clouston Hidrotic Ectodermal Dysplasia Maps to the Pericentromeric Region of Chromosome 13q von Kibar, Zoha, Der Kaloustian, Vazken M., Brais, Bernard, Hani, Valerie, Fraser, F. Clarke, Rouleau, Guy A.

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Costello syndrome von Der Kaloustian, Vazken M., Moroz, Brenda, McIntosh, Nathalie, Watters, A. Kevin, Blaichman, Shirley

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Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10 von Wayne, Sigrid, Der Kaloustian, Vazken M., Schloss, Melvin, Polomeno, Robert, Scott, Daryl A., Hejtmancik, J. Fielding, Sheffield, Val C., Smith, Richard J. H.

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Acute airway obstruction in Hunter syndrome von Yoskovitch, Adi, Tewfik, Ted L, Brouillette, Robert T, Schloss, Melvin D, Der Kaloustian, Vazken M

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A Radiation Hybrid Map of 48 Loci Including the Clouston Hidrotic Ectodermal Dysplasia Locus in the Pericentromeric Region of Chromosome 13q von Kibar, Zoha, Lafrenière, Ronald G., Chakravarti, Aravinda, Wang, Jia-Chi, Chevrette, Mario, Der Kaloustian, Vazken M., Rouleau, Guy A.

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New clinical genetics—2nd edition von Der Kaloustian, Vazken M

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Clonal lines of aneuploid cells in Rothmund-Thomson syndrome von Der Kaloustian, Vazken M., McGill, James J., Vekemans, Michel, Kopelman, Hinda R.

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The Camera-Marugo-Cohen syndrome: Report of two new patients von Lambert, Deborah M., Watters, Gordon, Andermann, Frederick, Der Kaloustian, Vazken M.

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Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: A new syndrome von Der Kaloustian, Vazken M., McIntosh, Nathalie, Silver, Kenneth, Blaichman, Shirley, Halal, Fahed

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Fetal alcohol syndrome and bilateral tibial exostoses: a case report von AZOUZ, E. M, KAVIANIAN, G, DER KALOUSTIAN, V. M

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Linkage analysis of the Nail-Patella syndrome von CAMPEAU, E, WATKINS, D, ROULEAU, G. A, BABUL, R, BUCHANAN, J. A, MESCHINO, W, DER KALOUSTIAN, V. M

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