Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations von Luciani, J J, de Mas, P, Depetris, D, Mignon-Ravix, C, Bottani, A, Prieur, M, Jonveaux, P, Philippe, A, Bourrouillou, G, de Martinville, B, Delobel, B, Vallee, L, Croquette, M-F, Mattei, M-G

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Attenuated presentation of ataxia-telangiectasia with familial cancer history von Simonin, C., Devos, D., Vuillaume, I., de Martinville, B., Sablonnière, B., Destée, A., Stoppa-Lyonnet, D., Defebvre, L.

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Single-Copy Sequence Hybridizes to Polymorphic and Homologous Loci on Human X and Y Chromosomes von Page, David, de Martinville, Berengere, Barker, David, Wyman, Arlene, White, Ray, Francke, Uta, Botstein, David

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Localization of the Human OB Gene (OBS) to Chromosome 7q32 by Fluorescence in Situ Hybridization von Geffroy, Sandrine, De Vos, Piet, Staels, Bart, Duban, Bénédicte, Auwerx, Johan, de Martinville, Bérengère

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J - 36 Mononeuropathie multiple et hypocholestérolémie von Sillaire, A., Stojkovic, T., Lacour, A., Zephir, H., De Martinville, B., Vermersch, P.

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Sex reversal and diaphragmatic hernia in phenotypically female sibs with normal XY chromosomes von MANOUVRIER-HANU, S, BESSON, R, COUSIN, L, JEANPIERRE, C, KACET, N, CARTIGNY, M, DEVISME, L, STORME, L, DE MARTINVILLE, B, LEQUIEN, P

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Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome von FRANCKE, U, OCHS, H. D, WEDGWOOD, R. J, DE MARTINVILLE, B, GIACALONE, J, LINDGREN, V, DISTECHE, C, PAGON, R. A, HOFKER, M. H, VAN OMMEN, G.-J. B, PEARSON, P. L

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A novel missense mutation in the exon containing the putative ornithine-binding domain of the OTC enzyme in a female von Demmer, Laurie A., Kim, Jean M., de Martinville, Berengere, Dowton, S. Bruce

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Oncogene from Human EJ Bladder Carcinoma is Located on the Short Arm of Chromosome 11 von De Martinville, Bérengère, Giacalone, Joseph, Shih, Chiaho, Weinberg, Robert A., Francke, Uta

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Further example of a patient with Prader-Willi and Klinefelter syndromes of different parental origins von Geffroy, Sandrine, Evrard, Valérie, Taufour, Dominique, Vanderbecken, Stéphane, de Martinville, Bérengère

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The Human Fatty Acid Transport Protein-1 (SLC27A1; FATP-1) cDNA and Gene: Organization, Chromosomal Localization, and Expression von Martin, Geneviève, Nemoto, Masami, Gelman, Laurent, Geffroy, Sandrine, Najib, Jamila, Fruchart, Jean-Charles, Roevens, Peter, de Martinville, Bérengère, Deeb, Samir, Auwerx, Johan

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Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14 von de Martinville, B, Wyman, A R, White, R, Francke, U

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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus von DE MARTINVILLE, B, KUNKEL, L. M, FRANCKE, U, BRUNS, G, MORLE, F, KOENIG, M, MANDEL, J. L, HORWICH, A, LATT, S. A, GUSELLA, J. F, HOUSMAN, D

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DNA analysis of first-trimester chorionic villous biopsies: test for maternal contamination von de Martinville, B, Blakemore, K J, Mahoney, M J, Francke, U

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Prenatal diagnosis of severe factor vii deficiency using mutation detection and linkage analysis von Giansily‐Blaizot, Muriel, Aguilar‐Martinez, Patricia, Mazurier, Claudine, Cneude, Fabrice, Goudemand, Jenny, Schved, Jean‐Francois, De Martinville, Berengère

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The Human Gene for the β Subunit of Nerve Growth Factor is Located on the Proximal Short Arm of Chromosome 1 von Francke, Uta, De Martinville, Berengere, Coussens, Lisa, Ullrich, Axel

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Sex reversal and diaphragmatic hernia in phenotypicaly female sibs with normal XY chromosomes von Manouvrier-Hanu, S, Besson, R, Cousin, L, Jeanpierre, C, Kacet, N, Cartigny, M, Devisme, L, Storme, L, De Martinville, B, Lequien, P

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Human Ornithine Transcarbamylase Locus Mapped to Band Xp21.1 near the Duchenne Muscular Dystrophy Locus von Lindgren, Valerie, De Martinville, Bérengère, Horwich, Arthur L., Rosenberg, Leon E., Francke, Uta

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The c-Ha-ras1, insulin and β-globin loci map outside the deletion associated with aniridia-Wilms' tumour von de Martinville, Bérengère, Francke, Uta

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Regional assignments of three polymorphic DNA segments on human chromosome 15 von Brissenden, J. E., Page, D. C., de Martinville, B., Trowsdale, J., Botstein, D., Francke, U., Lalouel, J. M.

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