Search Results - "Allderdice, P W"

The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26 by Allderdice, P W, Gardner, H A, Galutira, D, Lockridge, O, LaDu, B N, McAlpine, P J

“…Human tissues have two distinct cholinesterase activities: acetylcholinesterase and butyrylcholinesterase. Acetylcholinesterase functions in the transmission…”
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Highly repetitive DNA in the baleen whale genera Balaenoptera and Megaptera by ARNASON, U, ALLDERDICE, P. W, LIEN, J, WIDEGREN, B

“…Three non-cross-hybridizing highly repetitive DNA components were studied in six whalebone and two toothed whale species. In one of the components, composition…”
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Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9 by ALLDERDICE, P. W, KAITA, H, LEWIS, M, MCALPINE, P. J, WONG, P, ANDERSON, J, GIBLETT, E. R

“…Cytogenetic, enzyme dosage, serological, and electrophoretic analyses of blood samples from members of three Newfoundland kindreds in which one specific…”
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Duplication 9q34 syndrome by ALLDERDICE, P. W, EALES, B, ONYETT, H, SPRAGUE, W, HENDERSON, K, LEFEUVRE, P. A, PAL, G

“…Phenotypic, karyotypic, and developmental homology between affected children of carriers of an inverted insertion (9) (q22.1q34.3q34.1) led to recognition of a…”
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The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs by MCALPINE, P. J, DIXON, M, ALLDERDICE, P. W, LOCKRIDGE, O, LA DU, B. N

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HaeIII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP) by GALUTIRA, D, ALLDERDICE, P. W, DAVIDSON, W. S

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Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity by CONNOLLY, M. J, PAYNE, R. H, JOHNSON, G, GALLIE, B. L, ALLDERDICE, P. W, MARSHALL, W. H, LAWTON, R. D

“…We report an example of four generation familial retinoblastoma in which there are three distinct categories of RB gene expression: frank retinoblastoma,…”
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A New low incidence red cell antigen, NFLD by LEWIS, M, KAITA, H, ALLDERDICE, P. W, BERGREN, M, MCALPINE, P. J

“…A "new" low incidence red cell antigen, NFLD, is described. It was found in a Caucasian family and is inherited as an autosomal dominant. The antigen is not…”
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Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells by Miller, O. J., Allderdice, P. W., Miller, D. A., Breg, W. R., Migeon, B. R.

“…The human chromosome retained in a hybrid clone derived from human cells and a mouse line deficient in thymidine kinase has the quinacrinefluorescence pattern…”
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Cytological Mapping of Human X-Linked Genes by Use of Somatic Cell Hybrids Involving an X-Autosome Translocation by Grzeschik, K. H., Allderdice, P. W., Grzeschik, A., Opitz, J. M., Miller, O. J., Siniscalco, M.

“…Man-mouse and man-Syrian hamster somatic hybrid cell lines were prepared by fusion of mouse A9 or hamster TG2 cells, which are deficient in…”
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Identification of the Mouse Karyotype by Quinacrine Fluorescence, and Tentative Assignment of Seven Linkage Groups by Miller, O. J., Miller, D. A., Kouri, R. E., Allderdice, P. W., Dev, V. G., Grewal, M. S., Hutton, J. J.

“…A karyotype of the mitotic chromosomes of the house mouse has been prepared based upon quinacrine fluorescence patterns. All 19 pairs of autosomes and the X…”
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Human chromosomes in 18 man-mouse somatic hybrid cell lines analysed by quinacrine fluorescence by Allderdice, P W, Miller, O J, Pearson, P L, Klein, G, Harris, H

“…Chromosome studies were done on 18 somatic hybrid cell lines produced by fusing cells of the mouse A 9 line with cells of the human Daudi lymphoblastoid line…”
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Reversible dysfunction of T-lymphocytes in common variable immunodeficiency by Marshall, W. H, Allderdice, P. W, Edstrom, H. W, Newton, R. M, Pike, E

“…A 30-year-old man with recurrent sinopulmonary infections, eventually fatal, was found to have common variable immunodeficiency. In addition to low serum…”
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Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence by Allderdice, P W, Miller, O J, Miller, D A, Warburton, D, Pearson, P L, Klein, G, Harris, H

“…The fluorescent banding patterns of quinacrine-stained metaphase chromosomes have been studied in 2 related mouse cell lines, A9 and a malignant derivative of…”
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Complementation by two non-homologous recombinant chromosomes 3 by Allderdice, P W, Ali, M, McAlpine, P J

“…The first example known to us of complementation by two non-homologous chromosomes 3 is present in the karyotype of a phenotypically normal brother of an…”
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Quinacrine Fluorescence Patterns of Human D Group Chromosomes by MILLER, D. A, ALLDERDICE, P. W, MILLER, O. J, BREG, W. R

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The 13q-deletion syndrome by Allderdice, P W, Davis, J G, Miller, O J, Klinger, H P, Warburton, D, Miller, D A, Allen, Jr, F H, Abrams, C A, McGilvray, E

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A Study of the Chromosomes of the Normal Male Rabbit and Two Intersex Rabbits with Quinacrine Fluorescence and Giemsa Banding by Ducayen, M. B., Jagiello, G. M., Allderdice, P. W., Miller, W. A., Grey, R., Fang, J. S.

“…Two agonadal intersex rabbits were studied cytogenetically. The Quinacrine fluorescence and Giemsa banding patterns of normal male rabbit mitotic chromp somes…”
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QUINACRINE FLUORESCENT CHROMOSOME ANALYSIS OF THE SNELL TRANSLOCATION IN THE MOUSE by Miller, D. A, Allderdice, P. W, Kouri, R. E, Dev, V. G, Grewal, M. S, Miller, O. J, Hutton, J. J

“…The chromosomes involved in the T(2;4)Sn (formerly designated T(5;8) Sn) or Snell translocation in the mouse have been identified as numbers 2 and 4 by…”
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Method for locating the centromeres of mouse meiotic chromosomes and its application to T163H and T70H translocations by Dev, V G, Miller, D A, Allderdice, P W, Miller, O J

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