A new gene (DYX3) for dyslexia is located on chromosome 2 von Fagerheim, Toril, Raeymaekers, Peter, Tønnessen, Finn Egil, Pedersen, Marit, Tranebjærg, Lisbeth, Lubs, Herbert A

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Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene von Lubs, H, Abidi, F E, Echeverri, R, Holloway, L, Meindl, A, Stevenson, R E, Schwartz, C E

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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene von Schwartz, Charles E, Tarpey, Patrick S, Lubs, Herbert A, Verloes, Alain, May, Melanie M, Risheg, Hiba, Friez, Michael J, Futreal, P Andrew, Edkins, Sarah, Teague, Jon, Briault, Sylvain, Skinner, Cindy, Bauer-Carlin, Astrid, Simensen, Richard J, Joseph, Sumy M, Jones, Julie R, Gecz, Josef, Stratton, Michael R, Raymond, F Lucy, Stevenson, Roger E

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Renpenning syndrome comes into focus von Stevenson, Roger E., Bennett, C.W., Abidi, F., Kleefstra, T., Porteous, M., Simensen, R.J., Lubs, H.A., Hamel, B.C.J., Schwartz, C.E.

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A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58 von Abidi, F E, Holinski-Feder, E, Rittinger, O, Kooy, F, Lubs, H A, Stevenson, R E, Schwartz, C E

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Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene von Lebel, RR, May, M, Pouls, S, Lubs, HA, Stevenson, RE, Schwartz, CE

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A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25 von Cabezas, David A, Slaugh, Rachel, Abidi, Fatima, Arena, J Fernando, Stevenson, Roger E, Schwartz, Charles E, Lubs, Herbert A

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A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness von Jin, Hong, May, Melanie, Tranebjærg, Lisbeth, Kendall, Elaine, Fontán, Gumersindo, Jackson, John, Subramony, S.H., Arena, Fernando, Lubs, Herbert, Smith, Stephanie, Stevenson, Roger, Schwartz, Charles, Vetrie, David

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Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 ( MCT8) Gene von Schwartz, Charles E., May, Melanie M., Carpenter, Nancy J., Rogers, R. Curtis, Martin, Judith, Bialer, Martin G., Ward, Jewell, Sanabria, Javier, Marsa, Silvana, Lewis, James A., Echeverri, Roberto, Lubs, Herbert A., Voeller, Kytja, Simensen, Richard J., Stevenson, Roger E.

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Renpenning Syndrome Maps to Xp11 von Stevenson, Roger E., Arena, J. Fernando, Ouzts, Elizabeth, Gibson, Alice, Shokeir, M.H.K., Vnencak-Jones, Cindy, Lubs, Herbert A., May, M., Schwartz, Charles E.

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Suggestive linkage of developmental dyslexia to chromosome 1p34-p36 von Rabin, M., Wen, X.L., Hepburn, M., Lubs, H.A., Feldman, E., Duara, R.

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The Safety and Efficacy of Chorionic Villus Sampling for Early Prenatal Diagnosis of Cytogenetic Abnormalities von Rhoads, George G, Jackson, Laird G, Schlesselman, Sarah E, de la Cruz, Felix F, Desnick, Robert J, Golbus, Mitchell S, Ledbetter, David H, Lubs, Herbert A, Mahoney, Maurice J, Pergament, Eugene, Simpson, Joe Leigh, Carpenter, Robert J, Elias, Sherman, Ginsberg, Norman A, Goldberg, James D, Hobbins, John C, Lynch, Lauren, Shiono, Patricia H, Wapner, Ronald J, Zachary, Julia M

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I. The action of potassium permanganate upon 1-phenyl-3-thiourazole and 1-phenyl-thiomethylurazole. II. The tautomerism of 1-phenyl-5-oxy-4, 5-dihydro-3-triazolyl methyl sulphone.... von Lubs, H. A. 1891

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A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28 von Pai, G S, Hane, B, Joseph, M, Nelson, R, Hammond, L S, Arena, J F, Lubs, H A, Stevenson, R E, Schwartz, C E

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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor von Ramser, Juliane, Abidi, Fatima E., Burckle, Celine A., Lenski, Claus, Toriello, Helga, Wen, Gaiping, Lubs, Herbert A., Engert, Stefanie, Stevenson, Roger E., Meindl, Alfons, Schwartz, Charles E., Nguyen, Genevieve

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Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders von Plenge, Robert M., Stevenson, Roger A., Lubs, Herbert A., Schwartz, Charles E., Willard, Huntington F.

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Cytogenetic results from the U.S. collaborative study on CVS von Ledbetter, D. H., Zachary, J. M., Simpson, J. L., Golbus, M. S., Pergament, E., Jackson, L., Mahoney, M. J., Desnick, R. J., Schulman, J., Copeland, K. L., Verlinsky, Y., Yang-Feng, T., Schonberg, S. A., Babu, A., Tharapel, A., Dorfmann, A., Lubs, H. A., Rhoads, G. G., Fowler, S. E., De La Cruz, F.

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Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation von Stevenson, R E, Häne, B, Arena, J F, May, M, Lawrence, L, Lubs, H A, Schwartz, C E

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Inherited Mutations in PTEN That Are Associated with Breast Cancer, Cowden Disease, and Juvenile Polyposis von Lynch, Eric D., Ostermeyer, Elizabeth A., Lee, Ming K., Arena, J. Fernando, Ji, HanLee, Dann, Jamie, Swisshelm, Karen, Suchard, David, MacLeod, Patrick M., Kvinnsland, Stener, Gjertsen, Bjorn Tore, Heimdal, Ketil, Lubs, Herb, Møller, Pål, King, Mary-Claire

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A marker X chromosome von Lubs, H A

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