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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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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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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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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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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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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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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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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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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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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A marker X chromosome von Lubs, H A

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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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XLMR genes: Update 1990 von Neri, Giovanni, Gurrieri, Fiorella, Gal, Andreas, Lubs, Herbert A.

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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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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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Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study von Lubs, H. A., Ruddle, F. H.

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Gender Differences in the Severity of Adult Familial Dyslexia von Feldman, 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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Chromosome Polymorphism in American Negro and White Populations von LUBS, H. A, RUDDLE, F. H

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