Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome by 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 by 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 by Champion, KJ, Bunag, C, Estep, AL, Jones, JR, Bolt, CH, Rogers, RC, Rauen, KA, Everman, DB

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A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24 by 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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Serum α-fetoprotein levels in Beckwith-Wiedemann syndrome by Everman, David B., Shuman, Cheryl, Dzolganovski, Biljana, O’Riordan, Mary Ann, Weksberg, Rosanna, Robin, Nathaniel H.

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Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families by 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 by 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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P63 mutations are not a major cause of non-syndromic split hand/foot malformation by 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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Respiratory failure requiring extracorporeal membrane oxygenation after sodium phosphate enema intoxication by EVERMAN, David B, NITU, Mara E, JACOBS, Brian R

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

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