Familial testicular germ cell tumor: no associated syndromic pattern identified von Mueller, Christine M, Korde, Larissa A, McMaster, Mary L, Peters, June A, Bratslavsky, Gennady, Watkins, Rissah J, Ling, Alex, Kratz, Christian P, Wulfsberg, Eric A, Rosenberg, Philip S, Greene, Mark H

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Speech characteristics in the Kabuki syndrome von Upton, Sheila, Stadter, Carmella S., Landis, Pat, Wulfsberg, Eric A.

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Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome von Norris, R A, Scott, K K, Moore, C S, Stetten, G, Brown, C R, Jabs, E W, Wulfsberg, E A, Yu, J, Kern, M J

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Testing Children for Genetic Predispositions: Is it in Their Best Interest? von Hoffmann, Diane E., Wulfsberg, Eric A.

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The impact of genetic testing on primary care: where's the beef? von Wulfsberg, E A

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Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families von Wyszynski, D. F., Maestri, Nancy, McIntosh, Iain, Smith, E. Anne, Lewanda, Amy F., Garcia-Delgado, Constanza, Vinageras-Guarneros, Enrique, Wulfsberg, Eric, Beaty, Terri H.

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TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders von Splendore, Alessandra, Passos-Bueno, Maria Rita, Jabs, Ethylin Wang, Van Maldergem, Lionel, Wulfsberg, Eric A.

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Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries von LEANA-COX, J, LEVIN, S, SURANA, R, WULFSBERG, E, KEENE, C. L, RAFFEL, L. J, SULLIVAN, B, SCHWARTZ, S

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A complex chromosome rearrangement in a boy with autism von LOPREIATO, J. O, WULFSBERG, E. A

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Gorlin syndrome (naevoid basal cell carcinoma syndrome): Prenatal detection in a fetus with macrocephaly and ventriculomegaly von Hogge, W. Allen, Blank, Carol, Roochvarg, Linda B., Hogge, Joan S., Wulfsberg, Eric A., Raffel, Leslie J.

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Chondrodysplasia punctata: A boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders von Wulfsberg, Eric A., Curtis, Jerri, Jayne, Carol H.

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No Evidence of Linkage for Cleft Lip with or without Cleft Palate to a Marker Near the Transforming Growth Factor Alpha Locus in Two Populations von Wyszynski, Diego F., Maestri, Nancy, Lewanda, Amy F., McIntosh, Iain, Smith, E. Anne, García-Delgado, Constanza, Vinageras-Guarneros, Enrique, Wulfsberg, Eric, Beaty, Terri H.

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Genetic Heterogeneity among Craniosynostosis Syndromes: Mapping the Saethre-Chotzen Syndrome Locus between D7S513 and D7S516 and Exclusion of Jackson-Weiss and Crouzon Syndrome Loc... von Lewanda, Amy Feldman, Cohen, M.Michael, Jackson, Charles E., Taylor, Eugene W., Li, Xiang, Beloff, Michelle, Day, Donald, Clarren, Sterling K., Ortiz, Rosa, Garcia, Constanza, Hauselman, Ellyn, Figueroa, Alvaro, Wulfsberg, Eric, Wilson, Melba, Warman, Matthew L., Padwa, Bonnie L., Whiteman, David A.H., Mulliken, John B., Jabs, Ethylin Wang

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Chromosome 10qter deletion syndrome: A review and report of three new cases von Wulfsberg, Eric A., Weaver, Ramona P., Cunniff, Christopher M., Jones, Marilyn C., Jones, Kenneth Lyons

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Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15 von Olander, Erika, Stamberg, Judith, Steinberg, Lisa, Wulfsberg, Eric A.

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What's in a name? chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes von Wulfsberg, Eric A., Leana-Cox, Julie, Neri, Giovanni

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Antenatal diagnosis of lethal skeletal dysplasias von Tretter, Anne E., Saunders, Roger C., Meyers, Carol M., Dungan, Jeffrey S., Grumbach, Kathryn, Sun, Chen-Chih J., Campbell, Andrew B., Wulfsberg, Eric A.

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Is the autosomal dominant Opitz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2? von Wulfsberg, Eric A.

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Vertebral hypersegmentation in a case of the VATER association von Wulfsberg, Eric A., Phillips-Dawkins, Terri L., Thomas, Ronald L.

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Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literature von Leana-Cox, Julie, Pangkanon, Suthipong, Eanet, Karen R., Curtin, Martha S., Wulfsberg, Eric A.

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