Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome von Zarate, Y.A., Kalsner, L., Basinger, A., Jones, J.R., Li, C., Szybowska, M., Xu, Z.L., Vergano, S., Caffrey, A.R., Gonzalez, C.V., Dubbs, H., Zackai, E., Millan, F., Telegrafi, A., Baskin, B., Person, R., Fish, J.L., Everman, D.B.

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LADD syndrome is caused by FGF10 mutations von Milunsky, JM, Zhao, G, Maher, TA, Colby, R, Everman, DB

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Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome von Champion, KJ, Bunag, C, Estep, AL, Jones, JR, Bolt, CH, Rogers, RC, Rauen, KA, Everman, DB

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Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities von Hodge, J C, Mitchell, E, Pillalamarri, V, Toler, T L, Bartel, F, Kearney, H M, Zou, Y S, Tan, W H, Hanscom, C, Kirmani, S, Hanson, R R, Skinner, S A, Rogers, R C, Everman, D B, Boyd, E, Tapp, C, Mullegama, S V, Keelean-Fuller, D, Powell, C M, Elsea, S H, Morton, C C, Gusella, J F, DuPont, B, Chaubey, A, Lin, A E, Talkowski, M E

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A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24 von de Mollerat, Xavier J., Gurrieri, Fiorella, Morgan, Chad T., Sangiorgi, Eugenio, Everman, David B., Gaspari, Paola, Amiel, Jeanne, Bamshad, Michael J., Lyle, Robert, Blouin, Jean-Louis, Allanson, Judith E., Le Marec, Bernard, Wilson, Melba, Braverman, Nancy E., Radhakrishna, Uppala, Delozier-Blanchet, Celia, Abbott, Albert, Elghouzzi, Vincent, Antonarakis, Stylianos, Stevenson, Roger E., Munnich, Arnold, Neri, Giovanni, Schwartz, Charles E.

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P63 mutations are not a major cause of non-syndromic split hand/foot malformation von de Mollerat, X J, Everman, D B, Morgan, C T, Clarkson, K B, Rogers, R C, Colby, R S, Aylsworth, A S, Graham, J M, Stevenson, R E, Schwartz, C E

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Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules von EVERMAN, DAVID B., CASSIDY, SUZANNE B.

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Serum α-fetoprotein levels in Beckwith-Wiedemann syndrome von Everman, David B., Shuman, Cheryl, Dzolganovski, Biljana, O’Riordan, Mary Ann, Weksberg, Rosanna, Robin, Nathaniel H.

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DLG4-related synaptopathy: a new rare brain disorder von Rodríguez-Palmero, Agustí, Boerrigter, Melissa Maria, Gómez-Andrés, David, Aldinger, Kimberly A., Marcos-Alcalde, Íñigo, Popp, Bernt, Everman, David B., Lovgren, Alysia Kern, Arpin, Stephanie, Bahrambeigi, Vahid, Beunders, Gea, Bisgaard, Anne-Marie, Bjerregaard, V. A., Bruel, Ange-Line, Challman, Thomas D., Cogné, Benjamin, Coubes, Christine, de Man, Stella A., Denommé-Pichon, Anne-Sophie, Dye, Thomas J., Elmslie, Frances, Feuk, Lars, García-Miñaúr, Sixto, Gertler, Tracy, Giorgio, Elisa, Gruchy, Nicolas, Haack, Tobias B., Haldeman-Englert, Chad R., Haukanes, Bjørn Ivar, Hoyer, Juliane, Hurst, Anna C. E., Isidor, Bertrand, Soller, Maria Johansson, Kushary, Sulagna, Kvarnung, Malin, Landau, Yuval E., Leppig, Kathleen A., Lindstrand, Anna, Kleinendorst, Lotte, MacKenzie, Alex, Mandrile, Giorgia, Mendelsohn, Bryce A., Moghadasi, Setareh, Morton, Jenny E., Moutton, Sebastien, Müller, Amelie J., O’Leary, Melanie, Pacio-Míguez, Marta, Palomares-Bralo, Maria, Parikh, Sumit, Pfundt, Rolph, Pode-Shakked, Ben, Rauch, Anita, Repnikova, Elena, Revah-Politi, Anya, Ross, Meredith J., Ruivenkamp, Claudia A. L., Sarrazin, Elisabeth, Savatt, Juliann M., Schlüter, Agatha, Schönewolf-Greulich, Bitten, Shad, Zohra, Shaw-Smith, Charles, Shieh, Joseph T., Shohat, Motti, Spranger, Stephanie, Thiese, Heidi, Mau-Them, Frederic Tran, van Bon, Bregje, van de Burgt, Ineke, van de Laar, Ingrid M. B. H., van Drie, Esmée, van Haelst, Mieke M., van Ravenswaaij-Arts, Conny M., Verdura, Edgard, Vitobello, Antonio, Waldmüller, Stephan, Whiting, Sharon, Zweier, Christiane, Prada, Carlos E., de Vries, Bert B. A., Dobyns, William B., Reiter, Simone F., Gómez-Puertas, Paulino, Pujol, Aurora, Tümer, Zeynep

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Detection of free radicals during the cellular metabolism of adriamycin von Turner, Marvin J., Everman, David B., Ellington, Sharon P., Fields, Charles E.

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A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation von BABBS, Christian, HELLER, Raoul, EVERMAN, David B, CROCKER, Mark, TWIGG, Stephen R. F, SCHWARTZ, Charles E, GIELE, Henk, WILKIE, Andrew O. M

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Bipolar disorder associated with Klinefelter's syndrome and other chromosomal abnormalities von EVERMAN, D. B, STOUDEMIRE, A

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Evidence for superoxide formation during hepatic metabolism of tamoxifen von Turner, Marvin J., Fields, Charles E., Everman, David B.

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Short Report: LADD syndrome is caused by FGF10 mutations von Milunsky, J M, Zhao, G, Maher, T A, Colby, R, Everman, D B

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Microcephaly and Congenital Grouped Pigmentation of the Retinal Pigment Epithelium Associated with Submicroscopic Deletions of 13q33.3-q34 and 11p15.4 von Siddiqui, Ajaz M., Everman, David B., Rogers, R. Curtis, DuPont, Barbara R., Smith, Brooke T., Seaver, Laurie H., Morales, Augusto, Varn, Mary, Cohen, Bruce, Traboulsi, Elias I.

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Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families von Savarirayan, Ravi, White, Susan M., Goodman, Frances R., Graham Jr, John M., Delatycki, Martin B., Lachman, Ralph S., Rimoin, David L., Everman, David B., Warman, Matthew L.

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The FU gene and its possible protein isoforms von Østerlund, Torben, Everman, David B, Betz, Regina C, Mosca, Monica, Nöthen, Markus M, Schwartz, Charles E, Zaphiropoulos, Peter G, Toftgård, Rune

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Respiratory failure requiring extracorporeal membrane oxygenation after sodium phosphate enema intoxication von EVERMAN, David B, NITU, Mara E, JACOBS, Brian R

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The FU gene and its possible protein isoforms -: art. no. 49 von Osterlund, T, Everman, DB, Betz, RC, Mosca, M, Nöthen, MM, Schwartz, CE, Zaphiropoulos, PG, Toftgård, R

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Spinocerebellar ataxia type 29 due to mutations in ITPR1: A case series and review of this emerging congenital ataxia von Zambonin, JL, Bellomo, A, Ben-Pazi, H, Everman, DB, Frazer, LM, Geraghty, MT, Harper, AD, Jones, JR, Kamien, B, Kernohan, K, Koenig, MK, Lines, M, Palmer, EE, Richardson, R, Segel, R, Tarnopolsky, M, Vanstone, JR, Gibbons, M, Collins, A, Fogel, BL, Dudding-Byth, T, Boycott, KM, Palmer, Elizabeth

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