Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes von Keppler-Noreuil, K M, Carroll, A J, Finley, W H, Rutledge, S L

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The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32 von Drenth, Joost P.H., Finley, Wayne H., Breedveld, Guido J., Testers, Leon, Michiels, Jan J., Guillet, G., Taieb, Alain, Kirby, R. Lee, Heutink, Peter

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Pre-B Cell Leukemia Associated With Chromosome Translocation 1; 19 von Carroll, Andrew J., Crist, William M., Parmley, Richard T., Roper, Maryann, Finley, Max D. Cooper Wayne H.

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Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome von Han, Jian, Hsu, Chuancheih, Zhu, Zhou, Longshore, John W., Finley, Wayne H.

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Autosomal dominant erythromelalgia von Finley, W. H., Lindsey Jr, J. R., Fine, J.-D., Dixon, G. A., Burbank, M. K.

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Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23 von George, Alfred L., Knops, Judith F., Han, Jian, Finley, Wayne H., Knittie, Timothy J., Tamkun, Michael M., Brown, George B.

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A complex chromosome rearrangement resulting in trisomy 15q22→qter von Howard-Peebles, Patricia N, Scarbrough, Paula R, Sharpe, Joe, Finley, Wayne H, Finley, Sara C

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Survey of medical genetics personnel von Finley, W H, Finley, S C, Dyer, R L

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Decreased levels of amniotic fluid α-fetoprotein associated with Down syndrome von Davis, Richard O., Cosper, Paula, Huddleston, John F., Bradley, Edwin L., Finley, Sara C., Finley, Wayne H., Milunsky, Aubrey

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High resolution cytogenetic evaluation of couples with recurring fetal wastage von YANG-FENG, T. L, FINLEY, S. C, FINLEY, W. H, FRANCKE, U

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Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype von Krasikov, Natalie, Takaesu, Norma, Hassold, Terry, Knops, Judith F., Finley, Wayne H., Scarbrough, Paula

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Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence von Scarbrough, Paula R., Files, Beatrice, Carroll, Andrew J., Quinlan, R. William, Finley, Sara C., Finley, Wayne H.

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Congenital heart disease in infants with Down's syndrome von Wells, G L, Barker, S E, Finley, S C, Colvin, E V, Finley, W H

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A de novo 3p;8p unbalanced translocation resulting in partial dup(3p) and partial del(8p) von Scarbrough, P R, Carroll, A J, Finley, W H, Bridges, D R

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Effect of drugs on chromosome structure von Finley, WH

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Increased Chromosome Number of Rat Parotid Cells After Isoproterenol. von Schneyer, Charlotte A., Finley, Wayne H., Finley, Sara C.

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Birth defects surveillance: Jefferson County, Alabama, and Uppsala County, Sweden von Finley, W H, Gustavson, K H, Hall, T M, Hurst, D C, Barganier, C M, Wiedmeyer, J A

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An extra small metacentric chromosome in association with multiple congenital abnormalities von Finley, W H, Finley, S C, Monsky, D

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IgA ABSENCE ASSOCIATED WITH A RING-18 CHROMOSOME von Finley, SaraC, Finley, WayneH, Noto, ThomasA, Uchida, IreneA, Roddam, RoyF

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Suppression of Postnatal Changes in Spermatogenesis, Size, and Nucleic Acid Content of Rat Testis by Chronic Administration of Isoproterenol von Schneyer, Charlotte A., Luketic, Davor, Finley, Wayne H.

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