Mutations in the Gene Encoding the Inwardly-Rectifying Renal Potassium Channel, ROMK, Cause the Antenatal Variant of Bartter Syndrome: Evidence for Genetic Heterogeneity von Károlyi, Lothar, Konrad, Martin, Köckerling, Arnold, Ziegler, Andreas, Zimmermann, Dorthe K., Roth, Bernd, Wieg, Christian, Grzeschik, Karl-Heinz, Koch, Manuela C., Seyberth, Hannsjörg W., Vargas, Rosa, Forestier, Lionel, Jean, Genevieve, Deschaux, Michele, Rizzoni, Gian Franco, Niaudet, Patrick, Antignac, Corinne, Feldmann, Delphine, Lorridon, Frederique, Cougoureux, Emmanuel, Laroze, France, Alessandri, Jean-Luc, David, Louis, Saunier, Pascal, Deschenes, Georges, Hildebrandt, Friedhelm, Vollmer, Martin, Proesmans, Willem, Brandis, Matthias, van den Heuvel, Lambertus P. W. J., Lemmink, Henny H., Nillesen, Willy, Monnens, Leo A. H., Knoers, Nine V. A. M., Guay-Woodford, Lisa M., Wright, Christopher J., Madrigal, Gilbert, Hebert, Steven C.

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Identification of three novel mutations in the CFTR gene, R117P, ΔD192, and 3121-1G→A in four French patients von Feldmann, Delphine, Sardet, Anne, Cougoureux, Emmanuel, Plouvier, Elisabeth, Fontaine, Jean-Loup, Tournier, Guy, Aymard, Pierre

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Clinical evaluation of the CF(12)m cystic fibrosis DNA diagnostic kit von HOUDAYER, C, CAZENEUVE, C, COUGOUREUX, E, MAGNIER, C, TREDANO, M, AYMARD, P, GOOSSENS, M, FELDMANN, D

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Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P) von Houdayer, Claude, Bonaïti-Pellié, Catherine, Erguy, Caroline, Soupre, Véronique, Dondon, Marie-Gabrielle, Bürglen, Lydie, Cougoureux, Emmanuel, Couderc, Rémy, Vazquez, Marie-Paule, Bahuau, Michel

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Despite 'Spectacular' Drop in Infections, a Wary France Steps Cautiously von Nossiter, Adam

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Accessing Sustainable Quality Education in Rural Areas During Covid-19 in Anambra State, Nigeria von Ogbudinkpa, I. C.

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