Physical mapping of the holoprosencephaly critical region on chromosome 7q36 von Schinzel, Albert, Trask, Barbara J, van den Engh, Ger, Krauss, Celeste M, Pettenati, Mark J, Schindler, Detlef, Dietz-Band, Jeanne, Scherer, Stephen W, Tsui, Lap-Chee, Gurrieri, Fiorella, Muenke, Maximilian, Vergnaud, Gilles

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Familial Premature Ovarian Failure Due to an Interstitial Deletion of the Long Arm of the X Chromosome von Krauss, Celeste M, Turksoy, R. Nuran, Atkins, Leonard, McLaughlin, Cynthia, Brown, Laura G, Page, David C

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Prenatal Test for X-Linked Severe Combined Immunodeficiency by Analysis of Maternal X-Chromosome Inactivation and Linkage Analysis von Puck, Stirling M, Puck, Jennifer M, Krauss, Celeste M, Buckley, Rebecca H, Conley, Mary Ellen

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Ultrasound Detection of Fetal Aneuploidy in Patients With Elevated Maternal Serum Alpha- Fetoprotein von BARTH, WILLIAM H, FRIGOLETTO, FREDRIC D, KRAUSS, CELESTE M, MacMILLIN, MARTHA D, STRYKER, JANICE M, BENACERRAF, BERYL R

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Is fetal hyperechoic bowel on second-trimester sonogram an indication for amniocentesis ? von BROMLEY, B, DOUBILET, P, FRIGOLETTO, F. D, KRAUSS, C, ESTROFF, J. A, BENACERRAF, B. R

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Prenatal detection and mapping of a distal 8p deletion associated with congenital heart disease von Bhatia, Sangeeta N., Suri, Veena, Bundy, Albert, Krauss, Celeste M.

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Familial Premature Ovarian Failure due to an Interstitial Deletion of the Long Arm of the Chromosome von KRAUSS, CELESTE M, TURKSOY, NURAN R, ATKINS, LEONARD, MCLAUGHLIN, CYNTHIA, BROWN, LAURA G, PAGE, DAVID C

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In utero resolution of a fetal cystic hygroma in a male with a 46,XY karyotype and normal development at one year von Krauss, Celeste M., Beneceraff, Beryl

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Prenatal diagnosis of lissencephaly von Saltzman, Daniel H., Krauss, Celeste M., Goldman, Janet M., Benacerraf, Beryl R.

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Brief Report: Prenatal Test for X-Linked Severe Combined Immunodeficiency by Analysis of Maternal X-Chromosome Inactivation and Linkage Analysis von Puck, Jennifer M, Krauss, Celeste M, Puck, Stirling M, Buckley, Rebecca H, Conley, Mary Ellen

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Physical mapping of the holoprosencephaly critical region on chromosome 7q36 von Gurrieri, Fiorella, Trask, Barbara J, van den Engh, Ger, Krauss, Celeste M, Schinzel, Albert, Pettenati, Mark J, Schindler, Detlef, Dietz-Band, Jeanne, Vergnaud, Gilles, Scherer, Stephen W, Tsui, Lap-Chee, Muenke, Maximilian

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Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36 von Hatziioannou, Androniki G., Krauss, Celeste M., Lewis, Michael B., Halazonetis, Thanos D.

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Four siblings with similar malformations after exposure to phenytoin and primidone von Krauss, Celeste M., Holmes, Lewis B., VanLang, QuynhChi N., Keith, David A.

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Prenatal diagnosis of inverted duplicated 8p von Macmillin, Martha D., Suri, Veena, Lytle, Christia, Krauss, Celeste M.

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Four cases with hypoplastic thumbs and encephaloceles von Huang, Taosheng, Korson, Mark S., Krauss, Celeste, Holmes, Lewis B.

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Anomalies in an infant with Nager acrofacial dysostosis von Krauss, Celeste M., Hassell, Lewis A., Gang, David L., Opitz, John M., Reynolds, James F.

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Unilateral carpal bone deformity in mother and son von Krauss, Celeste M., Herman, Thomas E., Holmes, Lewis B., Opitz, John M., Reynolds, James F.

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Syndrome of telecanthus, hypertelorism, strabismus, and pes cavus in father and son von Krauss, Celeste M., Herman, Thomas E., Holmes, Lewis B., Opitz, John M., Reynolds, James F.

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Foundations for Decision Making von Intergovernmental Panel on Climate Change

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Transitional cell carcinoma arising in a pyelocaliceal cyst : An unusual cystic renal lesion with cytologic and imaging findings von FRIEDMAN, H. D, NSOULI, I. S, KRAUSS, D. J, VOHRA, S, POWERS, C. N

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