Arama Sonuçları - Ledbetter, D H

Minireview: cryptic translocations and telomere integrity. Yazar: Ledbetter, D H

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A common fragile site at Xq27: theoretical and practical implications. Yazar: Ledbetter, S A, Ledbetter, D H

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Fra(10)(q25): the BrdU effect is substitution-dependent. Yazar: Gollin, S M, Holmquist, G P, Ledbetter, D H

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Classical lissencephaly syndromes: does the face reflect the brain? Yazar: Allanson, J E, Ledbetter, D H, Dobyns, W B

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Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly. Yazar: Ledbetter, S A, Kuwano, A, Dobyns, W B, Ledbetter, D H

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Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity. Yazar: Cantú, E S, Nussbaum, R L, Airhart, S D, Ledbetter, D H

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Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines. Yazar: Lichter, P, Ledbetter, S A, Ledbetter, D H, Ward, D C

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Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndrome. Yazar: Kwiatkowski, D J, Aklog, L, Ledbetter, D H, Morton, C C

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The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1. Yazar: Goode, M E, vanTuinen, P, Ledbetter, D H, Daiger, S P

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Amniotic-fluid-cell-culture failure and syringe toxicity revisited. Yazar: Ledbetter, D H, Dumars, K W, Carpenter, R J, Caskey, C T

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Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment. Yazar: Reilly, D S, Lewis, R A, Ledbetter, D H, Nussbaum, R L

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An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]. Yazar: Kondoleon, S, van Tuinen, P, Ledbetter, D H, Vissing, H, Litt, M

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Cosmid 128 defines three RFLPs on chromosome 17q23-qter. [HGM9 no. D17S77] Yazar: Litt, M, Kondoleon, S, Vissing, H, van Tuinen, P, Ledbetter, D H

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Deletion and amplification of the HGPRT locus in Chinese hamster cells. Yazar: Fuscoe, J C, Fenwick, R G, Ledbetter, D H, Caskey, C T

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Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation. Yazar: Matsumoto, N, Pilz, D T, Fantes, J A, Kittikamron, K, Ledbetter, D H

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Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisation. Yazar: Kingston, H M, Ledbetter, D H, Tomlin, P I, Gaunt, K L

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Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization. Yazar: Kuwano, A, Ledbetter, S A, Dobyns, W B, Emanuel, B S, Ledbetter, D H

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Cytogenetic findings in a prospective series of patients with DiGeorge anomaly. Yazar: Greenberg, F, Elder, F F, Haffner, P, Northrup, H, Ledbetter, D H

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Cosmid 1-26 defines four RFLPs on chromosome 17q23-qter [HGM9 No. D17S20]. Yazar: Buroker, N E, Kondoleon, S, van Tuinen, P, Ledbetter, D H, Litt, M

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An anonymous single-copy clone, p55-B1, from chromosome 17 identifies a TaqI RFLP [HGM9 no. D17S86] Yazar: Litt, M, Buder, A, Vissing, H, van Tuinen, P, Ledbetter, D H

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