RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS von HSU, LILLIAN Y. F., YU, MING-TSUNG, NEU, RICHARD L., VAN DYKE, DANIEL L., BENN, PETER A., BRADSHAW, CHRISTY L., SHAFFER, LISA G., HIGGINS, RODNEY R., KHODR, GABRIEL S., MORTON, CYNTHIA C., WANG, HUNGSHU, BROTHMAN, ARTHUR R., CHADWICK, DIANNE, DISTECHE, CHRISTINE M., JENKINS, LAUREN S., KALOUSEK, DAGMAR K., PANTZAR, TAPIO J., WYATT, PHILIP

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Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations von Wallerstein, Robert, Yu, Ming-Tsung, Neu, Richard L., Benn, Peter, Lee Bowen, Catherine, Crandall, Barbara, Disteche, Christine, Donahue, Roger, Harrison, Betty, Hershey, Douglas, Higgins, Rodney R., Jenkins, Lauren S., Jackson-Cook, Colleen, Keitges, Elizabeth, Khodr, Gabriel, Lin, C. C., Luthardt, Frederick W., Meisner, Lorraine, Mengden, Gregory, Patil, Shivanand R., Rodriguez, Maria, Sciorra, Leonard J., Shaffer, Lisa G., Stetten, Gail, Van Dyke, Daniel L., Wang, Hungshu, Williams, Fran, Zaslav, Ann-Leslie, Hsu, Lillian Y. F.

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Experience With High- Z Plasma-Facing Materials and Extrapolation to Future Devices von Neu, R.L.

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PRENATAL CYTOGENETIC RESULTS FROM CASES REFERRED FOR 44 DIFFERENT TYPES OF ABNORMAL ULTRASOUND FINDINGS von SANFORD HANNA, JULIE, NEU, RICHARD L., LOCKWOOD, DAVID H.

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Cytogenetic analysis of 1375 amniotic fluid specimens from pregnancies with gestational age less than 14 weeks von Lockwood, David H., Neu, Richard L.

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Prenatal diagnosis of inv(X)(q12q28) in a male fetus von Neu, R L, Brar, H S, Koos, B J

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Experiences With Tungsten Plasma Facing Components in ASDEX Upgrade and JET von Neu, Rudolf Ludwig, Brezinsek, Sebastijan, Beurskens, Marc, Bobkov, Volodymyr, de Vries, Peter, Giroud, Carine, Joffrin, Emmanuel, Kallenbach, Arne, Matthews, Guy F., Mayoral, Marie-Line, Pautasso, Gabriella, Putterich, Thomas, Ryter, Francois, Schweinzer, Josef

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Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents von Neu, R L, Kousseff, B G, Hardy, D E, Essig, Y P, Miller, K L, Jervis, G A, Tedesco, T A

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Ultrasound identification of apparently normal male genitalia in a 46,X,+mar fetus von Neu, R L, O'Brien, W F, Kousseff, B G, Tedesco, T A, Farmelo, M J, Essig, Y P, Miller, K L, Nichols, P M

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Difficulties in prenatal detection of mosaic trisomy 8 von Hanna, Julie Sanford, Neu, Richard L., Barton, John R.

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A liveborn infant with tetraploidy von Lafer, C. Z., Neu, R. L., Opitz, John M., Reynolds, James F.

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Trisomy 17 detected in amniotic fluid cells but not in newborn infant von Butler, Merlin G., Neu, Richard L., Mitchell, Kay

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A case of cyclopia with D trisomy von Neu, Richard L., Grant, James F., Gardner, Lytt I.

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46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiency von Neu, R L, Stockman, J A, Spitzer, R E, Tomar, R H

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Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatin von Ashton-Prolla, Patricia, Gershin, Irina F., Babu, Arvind, Neu, Richard L., Zinberg, Randi E., Willner, Judith P., Desnick, Robert J., Cotter, Philip D.

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Disappearance of a 47,XX,C+ leucocyte cell line in an infant who had previously exhibited 46,XX-47,XX,C+ mosaicism von Neu, R L, Bargman, G J, Gardner, L I

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XYY WITH ABNORMAL GENITALIA von Carakushansky, Gerson, Neu, RichardL, Gardner, LyttI

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Fibroblast chromosome preparations von Kajii, T, Neu, R L, Gardner, L I

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XY-XYY mosaicism in prepubertal boy with tall stature, prognathism, and malformations of the hands von Kajii, T, Neu, R L, Gardner, L I

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A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77 von Neu, R L, Voorhess, M L, Gardner, L I

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