Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa von WESTBROOK, V. A, DIEKMAN, A. B, FLICKINGER, C. J, HERR, J. C, KLOTZ, K. L, KHOLE, V. V, VON KAP-HERR, C, GOLDEN, W. L, EDDY, R. L, SHOWS, T. B, STOLER, M. H, LEE, C.-Y. G

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Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion von SHASHI, V, GOLDEN, W. L, ALLINSON, P. S, HALLORAN BLANTON, S, VON KAP-HERR, C, KELLY, T. E

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Discordant phenotypes and 45,X/46,X,idic(Y) von Kelly, T E, Franko, J B, Rogol, A, Golden, W L

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Gonadoblastomas in 45,X/46,XY mosaicism: Analysis of Y chromosome distribution by fluorescence in situ hybridization von IEZZONI, J. C, VON KAP-HERR, C, GOLDEN, W. L, GAFFEY, M. J

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Human fertilin β: Identification, characterization, and chromosomal mapping of an ADAM gene family member von Vidaeus, Cecilia M., von Kap-Herr, Chris, Golden, Wendy L., Eddy, Roger L., Shows, Thomas B., Herr, John C.

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Genetic and phenotypic changes associated with the acquisition of tumorigenicity in human bladder cancer von Gildea, John J., Golden, Wendy L., Harding, Michael A., Theodorescu, Dan

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Interphase Fluorescence in Situ Hybridization for Trisomy 12 on Archival Ovarian Sex Cord-Stromal Tumors von Shashi, Vandana, Golden, Wendy L., von Kap-Herr, Christopher, Andersen, William A., Gaffey, Michael J.

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Assignment of the Human Growth Hormone-Releasing Hormone Receptor Gene (GHRHR) to 7p14 by in Situ Hybridization von Gaylinn, Bruce D., von Kap-Herr, Christopher, Golden, Wendy L., Thorner, Michael O.

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Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene von Huang, Taosheng, Lin, Angela E., Cox, Gerald F., Golden, Wendy L., Feldman, Gerald L., Ute, Moog, Schrander-Stumpel, Connie, Kamisago, Mitsuhiro, Vermeulen, Stefan J.T.

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Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes von Park, Vicki Murtif, Gustashaw, Karen M., Bilenker, Robert M., Golden, Wendy L.

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Malignant rhabdoid tumor of the kidney: Involvement of chromosome 22 von Shashi, Vandana, Lovell, Mark A., Von Kap-Herr, Christopher, Waldron, Peter, Golden, Wendy L.

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Acquisition of acoustic startle response in relation to growth and thyroid function in rats von Schneider, Bernard F., Golden, Wendy L.

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Choanal atresia in a patient with the deletion (9p) syndrome von Shashi, Vandana, Golden, Wendy L., Fryburg, Julie S.

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Interstitial deletion of 8q13.3→ 22.1 associated with craniosynostosis von Fryburg, Julie S., Golden, Wendy L.

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Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome von Fryburg, Julie S., Lin, Kant Y., Golden, Wendy L.

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Deletion (14) (q24.3q32.1): Evidence for a distinct clinical phenotype von Karnitis, Sue A., Burns, Kathy, Sudduth, Kathy W., Golden, Wendy L., Wilson, William G.

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Distal deletion of the short arm of chromosome 6 von Zurcher, Vickie L., Golden, Wendy L., Zinn, Arthur B.

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RARA and PML gene rearrangements in acute promyelocytic leukemia with complex translocations and atypical features von McKinney, Christopher D., Williams, Michael E., Golden, Wendy L., Gemma, Nicholas W., Swerdlow, Steven H.

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Cytogenetic Abnormalities in Primary Bronchopulmonary Leiomyosarcoma of Childhood von Schneider, Bernard F., Lovell, Mark A., Golden, Wendy L.

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Are the occasional aneuploid cells in peripheral blood cultures significant? von Wenger, Sharon L., Golden, Wendy L., Dennis, Suzanne P., Steele, Mark W.

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