Genetic variability of μ-opioid receptor in an obstetric population von LANDAU, Ruth, CAHANA, Alex, SMILEY, Richard M, ANTONARAKIS, Stylianos E, BLOUIN, Jean-Louis

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Mutations in the DNAH11 (Axonemal Heavy Chain Dynein type 11) Gene Cause One Form of Situs Inversus Totalis and Most Likely Primary Ciliary Dyskinesia von Bartoloni, Lucia, Blouin, Jean-Louis, Pan, Yanzhen, Gehrig, Corinne, Maiti, Amit K., Scamuffa, Nathalie, Rossier, Colette, Jorissen, Mark, Armengot, Miguel, Meeks, Maggie, Mitchison, Hannah M., Eddie M. K. Chung, Delozier-Blanchet, Celia D., Craigen, William J., Antonarakis, Stylianos E.

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Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III von LEVINSON, D. F, HOLMANS, P, NORTON, N, WILLIAMS, N. M, SCHWAB, S. G, LERER, B, MOWRY, B. J, SANDERS, A. R, ANTONARAKIS, S. E, BLOUIN, J.-L, DELEUZE, J.-F, MALLET, J, STRAUB, R. E, OWEN, M. J, WILDENAUER, D. B, GEJMAN, P. V, PULVER, A. E, LAURENT, C, KENDLER, K. S, WALSH, D

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Loss of LKB1 Kinase Activity in Peutz-Jeghers Syndrome, and Evidence for Allelic and Locus Heterogeneity von Mehenni, Hamid, Gehrig, Corinne, Nezu, Jun-ichi, Oku, Asuka, Shimane, Miyuki, Rossier, Colette, Guex, Nicolas, Blouin, Jean-Louis, Scott, Hamish S., Antonarakis, Stylianos E.

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A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q von Dauvilliers, Yves, Blouin, Jean-Louis, Neidhart, Elisabeth, Carlander, Bertrand, Eliaou, Jean-François, Antonarakis, Stylianos E., Billiard, Michel, Tafti, Mehdi

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The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position... von Radhakrishna, Uppala, Bornholdt, Dorothea, Scott, Hamish S., Patel, Uday C., Rossier, Colette, Engel, Hartmut, Bottani, Armand, Chandal, Divya, Blouin, Jean-Louis, Solanki, Jitendra V., Grzeschik, Karl-Heinz, Antonarakis, Stylianos E.

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A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24 von de Mollerat, Xavier J., Gurrieri, Fiorella, Morgan, Chad T., Sangiorgi, Eugenio, Everman, David B., Gaspari, Paola, Amiel, Jeanne, Bamshad, Michael J., Lyle, Robert, Blouin, Jean-Louis, Allanson, Judith E., Le Marec, Bernard, Wilson, Melba, Braverman, Nancy E., Radhakrishna, Uppala, Delozier-Blanchet, Celia, Abbott, Albert, Elghouzzi, Vincent, Antonarakis, Stylianos, Stevenson, Roger E., Munnich, Arnold, Neri, Giovanni, Schwartz, Charles E.

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Capital Gains Taxes and Equity Trading: Empirical Evidence von Blouin, Jennifer L., Raedy, Jana Smith, Shackelford, Douglas A.

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Genetic heterogeneity in schizophrenia : stratification of genome scan data using co-segregating related phenotypes von PULVER, A. E, MULLE, J, LASSETER, V. K, WOLYNIEC, P. S, THORNQULST, M. H, MCGRATH, J. A, NESTADT, G, SWARTZ, K. L, BLOUIN, J-L, DOMBROSKI, B, LIANG, K-Y, HOUSMAN, D. E, KAZAZIAN, H. H, ANTONARAKIS, S. E

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Prostate cancer is part of the hereditary non‐polyposis colorectal cancer (HNPCC) tumor spectrum von Soravia, Claudio, van der Klift, Heleen, Bründler, Marie‐Anne, Blouin, Jean‐Louis, Wijnen, Juul, Hutter, Pierre, Fodde, Riccardo, Delozier‐Blanchet, Célia

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Arg16 homozygosity of the β -adrenergic receptor improves the outcome after β -agonist tocolysis for preterm labor

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Peutz-Jeghers Syndrome: Confirmation of Linkage to Chromosome 19p13.3 and Identification of a Potential Second Locus, on 19q13.4 von Mehenni, Hamid, Blouin, Jean-Louis, Radhakrishna, Uppala, Bhardwaj, Shiv Shanker, Bhardwaj, Kamla, Dixit, V.B., Richards, Kent F., Bermejo-Fenoll, Ambrosio, Silva Leal, Antonio, Raval, Ranjan C., Antonarakis, Stylianos E.

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Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes von Pulver, Ann E., Lasseter, Virginia K., Kasch, Laura, Wolyniec, Paula, Nestadt, Gerald, Blouin, Jean-Louis, Kimberland, Michelle, Babb, Robert, Vourlis, Sophia, Chen, Haiming, Lalioti, Maria, Morris, Michael A., Karayiorgou, Maria, Ott, Jurg, Meyers, Deborah, Antonarakis, Stylianos E., Housman, David, Kazazian, Haig H.

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Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity von Blouin, J L, Meeks, M, Radhakrishna, U, Sainsbury, A, Gehring, C, Saïl, G D, Bartoloni, L, Dombi, V, O'Rawe, A, Walne, A, Chung, E, Afzelius, B A, Armengot, M, Jorissen, M, Schidlow, D V, van Maldergem, L, Walt, H, Gardiner, R M, Probst, D, Guerne, P A, Delozier-Blanchet, C D, Antonarakis, S E

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FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients von Fokstuen, Siv, Antonarakis, Stylianos E., Blouin, Jean-Louis

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Is genetic analysis useful in the routine management of hydatidiform mole? von Petignat, Patrick, Billieux, Marie‐Hélène, Blouin, Jean‐Louis, Dahoun, Sophie, Vassilakos, Pierre

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A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure von Lespinasse, J., North, M.O., Paravy, C., Brunel, M.J., Malzac, P., Blouin, J.L.

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No evidence for linkage between schizophrenia and markers at chromosome 15q13-14 von Curtis, Logos, Blouin, Jean-Louis, Radhakrishna, Uppala, Gehrig, Corinne, Lasseter, Virginia K., Wolyniec, Paula, Nestadt, Gerald, Dombroski, Beth, Kazazian, Haig H., Pulver, Ann E., Housman, David, Bertrand, Daniel, Antonarakis, Stylianos E.

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Pre‐eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genes von Billieux, M.‐H., Petignat, P., Fior, A., Mhawech, P., Blouin, J.‐L., Dahoun, S., Vassilakos, P.

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Schizophrenia susceptibility and chromosome 6p24-22 von Antonarakis, Stylianos E, Blouin, Jean-Louis, Pulver, Ann E, Wolyniec, Paula, Lasseter, Virginia K, Nestadt, Gerald, Kasch, Laura, Babb, Robert, Kazazian, Haig H, Dombroski, Beth, Kimberland, Michelle, Ott, Jurg, Housman, David, Karayiorgou, Maria, MacLean, Charles J

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