Prenatal diagnosis of thalidomide syndrome von Gollop, T. R., Eigier, A., Neto, J. Guidugli

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X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families von Visinoni, Átila F., de Souza, Ricardo L.R., Freire-Maia, Newton, Gollop, Thomaz R., Chautard-Freire-Maia, Eleidi A.

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Ophthalmological, skeletal, and cardiac abnormalities in sibs born to consanguineous parents: A new syndrome? von dos Santos, Rita de Cassia Stocco, Castro, Nelson H. C., Ferraz, Oilita Pereira, Walter-Moura, Janete, Mustachi, Zan, Pagnan, Nina A. B., Gollop, Thomaz R.

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Normal outcome after a 45,X/46,XX/ 46,X,i(Xq) CVS diagnosis von Gollop, T. R., de C. Pieri, P., Pagnan, N. A. B., Naccache, N. F., Bittencourt, E. A.

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Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome von Gollop, Thomaz R.

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The Tel Hashomer camptodactyly syndrome: Report of a new case and review of the literature von Pagnan, Nina Amalia Brancia, Gollop, Thomaz Rafael, Lederman, Henrique, Optiz, John M., Reynolds, James F.

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Odontoonychodysplasia with alopecia: A new pure ectodermal dysplasia with probable autosomal recessive inheritance von Pinheiro, Marta, Freire-Maia, Newton, Gollop, Thomaz R., Opitz, John M., Reynolds, James F.

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A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and... von Richieri-Costa, A., Colletto, G. M. D. D., Gollop, T. R., Masiero, D., Opitz, John M., Reynolds, James F.

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Prenatal ultrasound diagnosis of diastrophic dysplasia at 16 weeks von Gollop, Thomaz Rafael, Eigier, Alberto, Opitz, John M., Reynolds, James F.

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Frontofacionasal dysplasia: Evidence for autosomal recessive inheritance von Gollop, T. R., Kiota, M. M., Martins, R. M. M., Lucchesi, E. A., Alvarenga F0, E.

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Apparent bifurcatio of distal humerous with oligoectro-syndactyly von Gollop, Thomaz Rafael, Coates, Veronica

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Familial occurrence of bifid femur and monodactylous ectrodactyly von Gollop, T. R., Lucchesi, E., Martins, R. M. M., Nione, A. S., Optiz, John M.

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Prader-Willi habitus, osteopenia, and camptodactyly (Urban-Rogers-Meyer syndrome): A probable second report von Pagnan, Nina A. B., Gollop, Thomaz Rafael, Opitz, John M., Reynolds, James F.

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The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literature von Gollop, Thomaz Rafael, Fontes, Luiz Roberto, Opitz, John M., Reynolds, James F.

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The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family von Gollop, T. R., Colletto, G. M. D. D., Opitz, John M.

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Prenatal diagnosis of 48,XYY, + 21 ascertained through ultrasound anomalies von Gollop, Thomaz Rafael, Naccache, Nadyr F., Auler-Bittencourt, Eloisa, Hauschild, Decio, Eigier, Alberto, Zveibil, Deborah K.

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H-Y antigen generating and receptor systems in abnormal sexual development von Moreira-Filho, C. A., Frota-Pessoa, O., Vianna-Morgante, Angela M., Chu, T. H., Bisi, H., Gollop, T. R., Opitz, John M.

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Brief clinical report: distal arthrogryposis type II D in three generations of a Brazilian family von BRANCIA PAGNAN, N. A, GOLLOP, T. R

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Autosomal recessive anophthalmia with multiple congenital abnormalities-type Waardenburg von Richieri-Costa, A., Gollop, T. R., Otto, P. G., Opitz, John M.

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Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a brazilian family von Richieri-Costa, A., Gollop, Thomaz R., Colletto, G. M. D. D., Opitz, John M.

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