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

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Highly repetitive DNA in the baleen whale genera Balaenoptera and Megaptera von ARNASON, U, ALLDERDICE, P. W, LIEN, J, WIDEGREN, B

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Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9 von ALLDERDICE, P. W, KAITA, H, LEWIS, M, MCALPINE, P. J, WONG, P, ANDERSON, J, GIBLETT, E. R

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

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Duplication 9q34 syndrome von ALLDERDICE, P. W, EALES, B, ONYETT, H, SPRAGUE, W, HENDERSON, K, LEFEUVRE, P. A, PAL, G

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The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs von MCALPINE, P. J, DIXON, M, ALLDERDICE, P. W, LOCKRIDGE, O, LA DU, B. N

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

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A New low incidence red cell antigen, NFLD von LEWIS, M, KAITA, H, ALLDERDICE, P. W, BERGREN, M, MCALPINE, P. J

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Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells von Miller, O. J., Allderdice, P. W., Miller, D. A., Breg, W. R., Migeon, B. R.

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Cytological Mapping of Human X-Linked Genes by Use of Somatic Cell Hybrids Involving an X-Autosome Translocation von Grzeschik, K. H., Allderdice, P. W., Grzeschik, A., Opitz, J. M., Miller, O. J., Siniscalco, M.

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Identification of the Mouse Karyotype by Quinacrine Fluorescence, and Tentative Assignment of Seven Linkage Groups von Miller, O. J., Miller, D. A., Kouri, R. E., Allderdice, P. W., Dev, V. G., Grewal, M. S., Hutton, J. J.

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Human chromosomes in 18 man-mouse somatic hybrid cell lines analysed by quinacrine fluorescence von Allderdice, P W, Miller, O J, Pearson, P L, Klein, G, Harris, H

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Reversible dysfunction of T-lymphocytes in common variable immunodeficiency von Marshall, W. H, Allderdice, P. W, Edstrom, H. W, Newton, R. M, Pike, E

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Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence von Allderdice, P W, Miller, O J, Miller, D A, Warburton, D, Pearson, P L, Klein, G, Harris, H

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Complementation by two non-homologous recombinant chromosomes 3 von Allderdice, P. W., Ali, M., McAlpine, P. J.

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The 13q-deletion syndrome von 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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Quinacrine Fluorescence Patterns of Human D Group Chromosomes von MILLER, D. A, ALLDERDICE, P. W, MILLER, O. J, BREG, W. R

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Method for locating the centromeres of mouse meiotic chromosomes and its application to T163H and T70H translocations von Dev, V.G., Miller, D.A., Allderdice, P.W., Miller, O.J.

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

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QUINACRINE FLUORESCENT CHROMOSOME ANALYSIS OF THE SNELL TRANSLOCATION IN THE MOUSE von Miller, D. A, Allderdice, P. W, Kouri, R. E, Dev, V. G, Grewal, M. S, Miller, O. J, Hutton, J. J

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