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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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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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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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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Deletion (12)(q15q21.2) von Watson, M S, McAllister-Barton, L, Mahoney, M J, Breg, W R

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

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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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Fragile X in a Survey of 75 Autistic Males von Watson, M S, Leckman, J F, Annex, B, Breg, W R, Boles, D, Volkmar, F R, Cohen, D J, Carter, C

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Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15 von Schreck, R R, Breg, W R, Erlanger, B F, Miller, O J

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Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression von Gilbert, F, Balaban, G, Breg, W R, Gallie, B, Reid, T, Nichols, W

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Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells von Miller, O. J., Allderdice, P. W., Miller, D. A., Breg, W. R., Migeon, B. R.

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Maternal metaphases on direct chromosome preparation of first trimester decidua von Blakemore, K J, Samuelson, J, Breg, W R, Mahoney, M J

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An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79] von Murphy, P.D., Kidd, J.R., Breg, W.R., Ruddle, F.H., Kidd, K.K.

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Molecular and cytogenetic characterization of 9p- abnormalities von Teebi, Ahmad S., Gibson, Lisa, McGrath, James, Meyn, M. S., Breg, W. Roy, Yang-Feng, Teresa L.

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A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis von Blakemore, K J, Watson, M S, Samuelson, J, Breg, W R, Mahoney, M J

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Quinacrine Fluorescence for Identifying Metaphase Chromosomes, with Special Reference to Photomicrography von Breg, W. R.

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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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FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype von Chu, Thomas W., Teebi, Ahmad S., Gibson, Lisa, Breg, W. R., Yang-Feng, Teresa L.

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