Fetal Cystic Hygroma: Cause and Natural History von Chervenak, Frank A, Isaacson, Glenn, Blakemore, Karin J, Breg, W. Roy, Hobbins, John C, Berkowitz, Richard L, Tortora, Marge, Mayden, Kara, Mahoney, Maurice J

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Craniorachischisis in a Partially Trisomic 11 Fetus in a family with Reproductive Failure and a Reciprocal Translocation, t(6p+;11q−) von Wright, Yvonne M., Clark, William E., Breg, W. Roy

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CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS von Steele, MarkW, Roy Breg, W.

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Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14 von RABIN, M, WATSON, M, KIDD, V, WOO, S. L. C, BREG, W. R, RUDDLE, F. H

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Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype von Lahn, Bruce T, Ma, Nancy, Breg, W. Roy, Stratton, Robert, Surti, Urvashi, Page, David C

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Oocyte production in a turner syndrome patient with serologically detectable male antigen von Haseltine, Florence P., Breg, W.Roy, Genel, Myron

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Regulation of rRNA gene expression in a human familial 14p+ marker chromosome von Miller, D A, Breg, W R, Warburton, D, Dev, V G, Miller, O J

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21 Monosomy in a retarded female infant von Halloran, Katherine H., Breg, W. Roy, Mahoney, Maurice J.

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Presence of H-Y Antigen in Patients with Ullrich-Turner Syndrome and X-Chromosome Rearrangements von HASELTINE, FLORENCE P, DEPONTE, KATHLEEN K, BREG, W ROY, GENEL, MYRON

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XY Gonadal Dysgenesis Associated with the Congenital Nephrotic Syndrome von GERTNER, JOSEPH M, KAUSCHANSKY, ARIEH, GIESKER, DAVID W, SIEGEL, NORMAN J, BREG, ROY W, GENEL, MYRON

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Analysis of Human Y-Chromosome-Specific Reiterated DNA in Chromosome Variants von Kunkel, Louis M., Smith, Kirby D., Boyer, Samuel H., Borgaonkar, Digamber S., Wachtel, Stephen S., Miller, O. J., Breg, W. Roy, Jones, Howard W., Rary, Jack M.

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FAMILY COUNSELING IN DOWNS SYNDROME von Breg, W. Roy

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A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism von PAUL, R, DYKENS, E, LECKMAN, J. F, WATSON, M, BREG, W. R, COHEN, D. J

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Human c-fos Oncogene Mapped within Chromosomal Region 14q21 → q31 von Barker, P. E., Rabin, Mark, Watson, Michael, Breg, W. Roy, Ruddle, Frank H., Verma, Inder M.

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PRENATAL DETECTION OF TWO DIFFERENT MONOSOMIC CELL LINES BY CHORIONIC VILLUS SAMPLING von HSU, TE-YAO, LIOU, JUI-DER, COPEL, JOSHUA A., MAHONEY, MAURICE J., BREG, W. ROY, YANG-FENG, TERESA L.

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Fetal blood sampling and cytogenetic abnormalities von Liou, Jui-Der, Chen, Chih-Ping, Breg, W. Roy, Hobbins, John C., Mahoney, Maurice J., Yang-Feng, Teresa L.

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Evidence for methylation of inactive human rRNA genes in amplified regions von Tantravahi, U, Breg, W R, Wertelecki, V, Erlanger, B F, Miller, O J

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Mapping the Locus of the H-Y Gene on the Human Y Chromosome von Koo, Gloria C., Wachtel, Stephen S., Krupen-Brown, Karen, Mittl, Lillian R., Breg, W. Roy, Genel, Myron, Rosenthal, Ira M., Borgaonkar, Digamber S., Miller, Dorothy A., Tantravahi, Ramana, Schreck, Rhona R., Erlanger, Bernard F., Miller, Orlando J.

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Chromosome 3 duplication q/deletion p syndrome von Fineman, R M, Hecht, F, Ablow, R C, Howard, R O, Breg, W R

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Methods in Human Cytogenetics von Breg, W. Roy

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