Molecular cytogenetic insights to the phylogenetic affinities of the giraffe (Giraffa camelopardalis) and pronghorn (Antilocapra americana) von Cernohorska, Halina, Kubickova, Svatava, Kopecna, Olga, Kulemzina, Anastasia I, Perelman, Polina L, Elder, Frederick F. B, Robinson, Terence J, Graphodatsky, Alexander S, Rubes, Jiri

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Chromosomal evolution in tenrecs (Microgale and Oryzorictes, Tenrecidae) from the Central Highlands of Madagascar von Gilbert, C, Goodman, S. M, Soarimalala, V, Olson, L. E, O'Brien, P. C. M, Elder, F. F. B, Yang, F, Ferguson-Smith, M. A, Robinson, T. J

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Reversal of Left-Right Asymmetry: A Situs Inversus Mutation von Yokoyama, Takahiko, Copeland, Neal G., Jenkins, Nancy A., Montgomery, Charles A., Frederick F. B. Elder, Overbeek, Paul A.

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Chromosome painting among Proboscidea, Hyracoidea and Sirenia: support for Paenungulata (Afrotheria, Mammalia) but not Tethytheria von Pardini, A. T., O'Brien, P. C. M., Fu, B., Bonde, R. K., Elder, F. F. B., Ferguson-Smith, M. A., Yang, F., Robinson, T. J.

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Patterns of Chromosomal Evolution in Sigmodon, Evidence from Whole Chromosome Paints von Swier, V.J., Bradley, R.D., Rens, W., Elder, F.F.B., Baker, R.J.

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Lagomorphs (rabbits, pikas and hares) do not use telomere-directed replicative aging in vitro von Forsyth, Nicholas R., Elder, Frederick F.B., Shay, Jerry W., Wright, Woodring E.

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45,X/46,X, + r(X) can have a distinct phenotype different from Ullrich-Turner syndrome von Grompe, M., Rao, N., Elder, F. F. B., Caskey, C. T., Greenberg, F.

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A molecular cytogenetic analysis of X chromosome repatterning in the Bovidae: transpositions, inversions, and phylogenetic inference von Robinson, T.J., Harrison, W.R., Ponce de León, F.A., Davis, S.K., Elder, F.F.B.

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis von Sohocki, Melanie M., Bowne, Sara J., Sullivan, Lori S., Blackshaw, Seth, Cepko, Constance L., Payne, Annette M., Bhattacharya, Shomi S., Khaliq, Shagufta, Qasim Mehdi, S., Birch, David G., Harrison, Wilbur R., Elder, Frederick F.B., Heckenlively, John R., Daiger, Stephen P.

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Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome von Shapira, Stuart K., McCaskill, Christopher, Northrup, Hope, Spikes, Aimee S., Elder, F.F.B., Sutton, V. Reid, Korenberg, Julie R., Greenberg, Frank, Shaffer, Lisa G.

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Chromosomal evolution in the vlei rat, Otomys irroratus (Muridae: Otomyinae): a compound chromosomal rearrangement separates two major cytogenetic groups von Rambau, R.V., Elder, F.F.B., Robinson, T.J.

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Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia von Hecht, Jacqueline T., Nelson, Laura D., Crowder, Eric, Wang, Yang, Elder, Frederick F.B., Harrison, Wilbur R., Francomano, Clair A., Prange, Christa K., Lennon, Gregory G., Deere, Michelle, Lawler, Jack

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Multiple common fragile sites are expressed in the genome of the laboratory rat von ROBINSON, T. J, ELDER, F. F. B

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PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM von CHRISTIAN, SUSAN L., SMITH, ANN C. M., MACHA, MICHELLE, BLACK, SUSAN H., ELDER, FREDERICK F. B., JOHNSON, JAMIE M.-P., RESTA, ROBERT G., SURTI, URVASHI, SUSLAK, LORRAINE, VERP, MARION S., LEDBETTER, DAVID H.

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Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome von Lu, Wei, Phillips, Carrie L., Killen, Paul D., Hlaing, Tommy, Harrison, Wilbur R., Elder, F.F.B., Miner, Jeffrey H., Overbeek, Paul A., Meisler, Miriam H.

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Identification of abnormal chromosomal complement in formalin-fixed, paraffin-embedded placental tissue von Cowles, Tracy A., Elder, Frederick F. B., Taylor, Suzanne

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Rodent common fragile sites: are they conserved: evidence from mouse and rat von ELDER, F. F. B, ROBINSON, T. J

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Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse von MORGAN, D, TURNPENNY, L, ELDER, F. F. B, PENMAN-SPLITT, M, OVERBEEK, P, STRACHAN, T, GOODSHIP, J, DAI, W, MAJUMDER, K, MATTHEWS, L, GARDNER, A, SCHUSTER, G, VIEN, L, HARRISON, W

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Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4 von ALTHERR, M. R, BENGTSSON, U, ELDER, F. F. B, LEDBETTER, D. H, WASMUTH, J. J, MCDONALD, M. E, GUSELLA, J. F, GREENBERG, F

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Cytogenetic findings in a prospective series of patients with DiGeorge anomaly von GREENBERG, F, ELDER, F. F. B, HAFFNER, P, NORTHRUP, H, LEDBETTER, D. H

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