Simpson-golabi-behmel syndrome: An X-linked encephalo-tropho-schisis syndrome von Neri, G., Marini, R., Cappa, M., Borrelli, P., Opitz, J.M.

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Studies of Malformation Syndromes XXVA von Motl, Mary Lou, Opitz, J.M.

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Genetics of tethered cord "syndrome" The FG syndrome von Opitz, J.M.

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The Fg Syndrome: From 1974–2004 von Smith, J.F., Wayment, R.O., Opitz, J.M.

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Transitory hypogammaglobulinemia of infancy in FG syndrome von Finocchi, A., Palma, P., Rossi, P., Opitz, J.M., Neri, G.

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A close relationship to Smith-Lemli-Opitz (RSH) patients positively correlates with an increased incidence of high cholesterol, late-onset diabetes, and infertility; and negatively... von Poss, A.F., Metherall, J.E., Opitz, J.M.

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Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patients von Kavamura, M.I., Zollino, M., Lecce, R., Murdolo, M., Brunoni, D., Alchorne, M.M.A., Opitz, J.M., Neri, G.

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Errors of morphogenesis: Concepts and terms von Spranger, J., Benirschke, K., Hall, J.G., Lenz, W., Lowry, R.B., Opitz, J.M., Pinsky, L., Schwarzacher, H.G., Smith, D.W.

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The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients an... von Schinzel, A., Schmid, W., Fraccaro, M., Tiepolo, L., Zuffardi, Orsetta, Opitz, J.M., Lindsten, J., Zetterqvist, P., Enell, H., Baccichetti, C., Tenconi, R., Pagon, RobertaA

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FEMINISING TESTES SYNDROME von Opitz, J.M

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Phenotypic mapping and clinical ideology von Lurie, Iosif W., Opitz, John M.

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Noonan's syndrome in girls: A genocopy of the Ullrich-Turner syndrome von Opitz, J.M., Summitt, R.L., Sarto, G.E.

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Cytogenetic investigations of an infant with a translocation chromosome of the Townes-Ziegler type von Opitz, J.M., Waisman, H.A., Hunter, R.E.

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Hypertelorism and hypospadias, a newly recognized hereditary malformation syndrome von Opitz, J.M., Smith, D.W., Summitt, R.L.

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SEQUENTIAL FETUS-FETUS INTERACTION AND C.N.S. DEFECTS von Durkin, M.V., Kaveggia, E.G., Pendleton, E., Opitz, J.M.

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TRISOMY-20 SYNDROME IN MAN von Pallister, P.D., Herrmann, J., Meisner, L.F., Inhorn, S.L., Opitz, J.M.

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TWINNING AND ILLEGITIMACY IN C.N.S. DEFECTS von Durkin, M.V., Kaveggia, E.G., Pendleton, E., Opitz, J.M.

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BRACHMANN/DE LANGE SYNDROME von Opitz, J.M., Segal, A.T., Lehrke, R., Nadler, H.

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DEVELOPMENTAL MIXOPLOIDY AND TRISOMY-20 SYNDROME von Meisner, L.F., Pallister, P.D., Inhorn, S.L., Herrmann, J., Opitz, J.M.

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Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility von Astuti, Dewi, Morris, Mark R, Cooper, Wendy N, Staals, Raymond H J, Wake, Naomi C, Fews, Graham A, Gill, Harmeet, Gentle, Dean, Shuib, Salwati, Ricketts, Christopher J, Cole, Trevor, van Essen, Anthonie J, van Lingen, Richard A, Neri, Giovanni, Opitz, John M, Rump, Patrick, Stolte-Dijkstra, Irene, Müller, Ferenc, Pruijn, Ger J M, Latif, Farida, Maher, Eamonn R

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