Gestalt diagnosis of children with dysmorphism - Necessity for establishing genetic diagnostic approach von Sarker, Shaoli, Mahbub, Mustafa, Azam, A. Z. M., Quaderi, H. R., Kanta, S. I., Ahmad, Fayaza

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Unmet Diagnostic and Therapeutic Opportunities for Chronic Obstructive Pulmonary Disease in Low- and Middle-Income Countries von Florman, Katia E H, Siddharthan, Trishul, Pollard, Suzanne L, Alupo, Patricia, Barber, Julie A, Chandyo, Ram K, Flores-Flores, Oscar, Kirenga, Bruce, Mendes, Renata Gonçalves, Miranda, J Jaime, Mohan, Sakshi, Ricciardi, Federico, Rykiel, Natalie A, Sharma, Arun K, Wosu, Adaeze C, Checkley, William, Hurst, John R

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Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 von Quaderi, Nandita A., Schweiger, Susann, Gaudenz, Karin, Franco, Brunella, Rugarli, Elena I., Berger, Wolfgang, Feldman, George J., Volta, Manuela, Andolfi, Grazia, Gilgenkrantz, S., Marion, Robert W., Hennekam, Raoul C.M., Opitz, John M., Muenke, Maximilian, Ropers, Hilger H., Ballabio, Andrea

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The Mouse Mid1 Gene: Implications for the Pathogenesis of Opitz Syndrome and the Evolution of the Mammalian Pseudoautosomal Region von Dal Zotto, Laura, Quaderi, Nandita A., Elliott, Rosemary, Lingerfelter, Patricia A., Carrel, Laura, Valsecchi, Valentina, Montini, Eugenio, Yen, Chao-Huang, Chapman, Verne, Kalcheva, Iveta, Arrigo, Giulia, Zuffardi, Orsetta, Thomas, Sushma, Willard, Huntington F., Ballabio, Andrea, Disteche, Christine M., Rugarli, Elena I.

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Differential Expression Pattern of XqPAR-Linked Genes SYBL1 and IL9R Correlates with the Structure and Evolution of the Region von D'Esposito, Maurizio, Matarazzo, Maria Rosaria, Ciccodicola, Alfredo, Strazzullo, Maria, Mazzarella, Richard, Quaderi, Nandita A., Fujiwara, Hiroyuki, Ko, Minoru S. H., Rowe, Lucy B., Ricco, Angela, Archidiacono, Nicoletta, Rocchi, Mariano, Schlessinger, David, D'Urso, Michele

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Genetic and Physical Mapping of a Gene Encoding a Methyl CpG Binding Protein, Mecp2, to the Mouse X Chromosome von Quaderi, N.A., Meehan, R.R., Tate, P.H., Cross, S.H., Bird, A.P., Chatterjee, A., Herman, G.E., Brown, S.D.M.

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Opitz G/BBB syndromes a defect of midline development, is due to mutations in a new RING finger gene on Xp22 von QUADERI, N. A, SCHWEIGER, S, MARION, R. W, HENNEKAM, R. C. M, OPITZ, J. M, MUENKE, M, ROPERS, H. H, BALLABIO, A, GAUDENZ, K, FRANCO, B, RUGARLI, E. I, BERGER, W, FELDMAN, G. J, VOLTA, M, ANDOLFI, G, GILGENKRANTZ, S

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Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome von Quaderi, NA, Meehan, R R, Tate, PH, Cross, SH, Bird, A P, Chatterjee, A, Herman, GE, Brown, SDM

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