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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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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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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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 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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Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse von Morgan, David, Turnpenny, Lee, Goodship, Judith, Dai, Weilie, Majumder, Kumud, Matthews, Lucy, Gardner, Alison, Schuster, Gaby, Vien, Long, Harrison, Wilbur, Elder, Frederick F.B., Penman-Splitt, Miranda, Overbeek, Paul, Strachan, Tom

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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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Expression of the rat liver carnitine palmitoyltransferase I (CPT-Ialpha) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization von Steffen, M L, Harrison, W R, Elder, F F, Cook, G A, Park, E A

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YAC rescue of downless locus mutations in mice von Majumder, K, Shawlot, W, Schuster, G, Harrison, W, Elder, F F, Overbeek, P A

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Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites von Sohocki, Melanie M., Sullivan, Lori S., Harrison, Wilbur R., Sodergren, Erica J., Elder, Frederick F.B., Weinstock, George, Tanase, Sumio, Daiger, Stephen P.

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Genomic DNA Sequence, Promoter Expression, and Chromosomal Mapping of Rat Muscle Carnitine Palmitoyltransferase I von Wang, Dachun, Harrison, Wilbur, Buja, L.Maximilian, Elder, Frederick F.B., McMillin, Jeanie 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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Cytogenetic characterization of three human and three rat medullary thyroid carcinoma cell lines von Cooley, Linda D, Elder, Frederick F.B, Knuth, Alexander, Gagel, Robert F

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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, Mehdi, S. Qasim, Birch, David G., Harrison, Wilbur R., Elder, Frederick F.B., Heckenlively, John R., Daiger, Stephen P.

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Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan von Deere, Michelle, Johnson, Jan, Garza, Sonya, Harrison, Wilbur R., Yoon, Sung-Joo, Elder, Frederick F.B., Kucherlapati, Raju, Hook, Magnus, Hecht, Jacqueline T.

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Leukocyte adhesion deficiency mimicking Hirschsprung disease von Rivera-Matos, Idalia R., Rakita, Robert M., Mariscalco, M.Michelle, Elder, Frederick F.B., Dreyer, Sherlene A., Cleary, Thomas G.

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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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Fetal blood sampling demonstrating chimerism in monozygotic twins discordant for sex and tissue karyotype (46,XY and 45,X) von Gonsoulin, Whitney, Copeland, Karen L., Carpenter Jr, Robert J., Hughes, Mark R., Elder, Frederick F. B.

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Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center von Pettigrew, A L, McCabe, E R, Elder, F F, Ledbetter, D H

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