Prader Willi/Angelman and DiGeorge/velocardiofacial syndrome deletions: Diagnosis by primed in situ labeling (PRINS) von Tharapel, Avirachan T., Kadandale, Jayarama S., Martens, Paula R., Wachtel, Stephen S., Wilroy Jr, R. Sid

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Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor von Pasteris, N G, Cadle, A, Logie, L J, Porteous, M E, Schwartz, C E, Stevenson, R E, Glover, T W, Wilroy, R S, Gorski, J L

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Localization of SRY by primed in situ labeling in XX and XY sex reversal von Kadandale, Jayarama S., Wachtel, Stephen S., Tunca, Yusuf, Wilroy Jr, R. Sid, Martens, Paula R., Tharapel, Avirachan T.

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Type 3 Pfeiffer syndrome with normal thumbs von Kerr, Natalie C., Sid Wilroy Jr, R., Kaufman, Robert A.

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Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative RhoRac guanine nucleotide exchange factor von German Pasteris, N., Cadle, Amy, Logie, Lindsay J., Porteous, Mary E.M., Schwartz, Charles E., Stevenson, Roger E., Glover, Thomas W., Sid Wilroy, R., Gorski, Jerome L.

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Deletion (X)(q26.1→q28) in a proband and her mother : molecular characterization and phenotypic-karyotypic deductions von THARAPEL, A. T, ANDERSON, K. P, SIMPSON, J. L, MARTENS, P. R, WILROY, R. S, LLERENA, J. C, SCHWARTZ, C. E

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Neoplasms in proteus syndrome von Gordon, Patricia L., Wilroy, R. Sid, Lasater, Olga E., Michael Jr, M. Cohen

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Deletion of chromosome 15pter→q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome von Qumsiyeh, Mazin B., Dalton, James D., Gordon, Patricia L., Wilroy, R. Sid, Tharapel, Avirachan T.

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Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS von Kadandale, Jayarama S., Wachtel, Stephen S., Tunca, Yusuf, Martens, Paula R., Wilroy, R. Sid, Tharapel, Avirachan T.

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REPORTS: Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity von Robin, Nathaniel H., Feldman, George J., Mitchell, Heather F., Lorenz, Peter, Wilroy, R.Sid, Zackal, Elaine H., AIIanson, Judith E., Reich, Elsa W., Pfeiffer, Rudolf A., Clarke, Lome A., Warmani, Matthew L., Mulliken, John B., Brueton, Louise A., Winter, Robin M., Price, R.Arien, Gasser, David L., Muenke, Maximilian

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Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counselling von Tharapel, Avirachan T., Ward, Jewell C., Wiggins, Lee, Wilroy Jr, R. Sid

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Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome von Pivnick, E K, Qumsiyeh, M B, Tharapel, A T, Summitt, J B, Wilroy, R S

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Hallermann-Streiff syndrome with hypopituitarism contributing to growth failure von Pivnick, Enikö K., Burstein, Stephen, Sid Wilroy, R., Kaufman, Robert A., Ward, Jewell C.

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High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement von Qumsiyeh, Mazin B., Wilroy, R. Sid, Peeden, Joseph N., Tharapel, Avirachan T.

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Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization von Zhao, Jian, Gordon, Patricia L., Wilroy Jr, R. Sid, Martens, Paula R., Tarleton, Jack, Shulman, Lee P., Simpson, Joe Leigh, Elias, Sherman, Tharapel, Avirachan T.

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Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with α-satellite DNA probes von Tharapel, Avirachan T., Qumsiyeh, Mazin B., Martens, Paula R., Tharapel, Sugandhi A., Dalton, James D., Ward, Jewell C., Wilroy Jr, R. Sid

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The telecanthus-hypospadias syndrome von Stevens, C A, Wilroy, R S

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Eludication of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation von Gordon, P L, Dalton, J D, Martens, PR, Tharapel, A T, Wilroy, R S

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Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative [formula omitted] guanine nucleotide exchange factor von German Pasteris, N., Cadle, Amy, Logie, Lindsay J., Porteous, Mary E.M., Schwartz, Charles E., Stevenson, Roger E., Glover, Thomas W., Sid Wilroy, R., Gorski, Jerome L.

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Linkage analysis in a family with the Opitz GBBB syndrome refines the location of the gene in Xp22 to a 4 cM region von May, Melanie, Huston, Sara, Wilroy, R. Sid, Schwartz, Charles

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