检索结果 - M.A. Ferguson‐Smith

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  1. 1
    Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations

    Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations 由 M.A. Ferguson‐Smith

    出版 1965
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  2. 2
    The Evolution of Sex Chromosomes and Sex Determination in Vertebrates and the Key Role of <i>DMRT1</i>

    The Evolution of Sex Chromosomes and Sex Determination in Vertebrates and the Key Role of <i>DMRT1</i> 由 M.A. Ferguson‐Smith

    出版 2006
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  3. 3
    Essential medical genetics

    Essential medical genetics 由 James Connor, M.A. Ferguson‐Smith

    出版 1994
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  4. 4
    Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

    Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma. 由 Eamonn R. Maher, John R. Yates, M.A. Ferguson‐Smith

    出版 1990
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  5. 5
    High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry.

    High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry. 由 Bryan D. Young, M.A. Ferguson‐Smith, R Sillar, E. Boyd

    出版 1981
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  6. 6
    Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

    Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion. 由 J. H. Renwick, Sarah Bundey, M.A. Ferguson‐Smith, Marion M Izatt

    出版 1971
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  7. 7
    Analysis of pilocytic astrocytoma by comparative genomic hybridization

    Analysis of pilocytic astrocytoma by comparative genomic hybridization 由 Despina Sanoudou, Ola Tingby, M.A. Ferguson‐Smith, V. Peter Collins, Nicholas Coleman

    出版 2000
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  8. 8
    Cloned DNA probes regionally mapped to human Chromosome 21 and their use in determining the origin of nondisjunction

    Cloned DNA probes regionally mapped to human Chromosome 21 and their use in determining the origin of nondisjunction 由 Gordon D. Stewart, Peter C. Harris, James R. Galt, M.A. Ferguson‐Smith

    出版 1985
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  9. 9
    The Triple-X Syndrome

    The Triple-X Syndrome 由 Andrew Johnston, M.A. Ferguson‐Smith, StanleyD. Handmaker, Howard W. Jones, Georgeanna S. Jones

    出版 1961
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  10. 10
    Non-homologous sex chromosomes in two species of the genus <i>Eigenmannia</i> (Teleostei: Gymnotiformes)

    Non-homologous sex chromosomes in two species of the genus <i>Eigenmannia</i> (Teleostei: Gymnotiformes) 由 Frederico Henning, Vladimir A. Trifonov, M.A. Ferguson‐Smith, Lurdes Foresti de Almeida-Toledo

    出版 2008
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  11. 11
    Epigenetic modifications on X chromosomes in marsupial and monotreme mammals and implications for evolution of dosage compensation

    Epigenetic modifications on X chromosomes in marsupial and monotreme mammals and implications for evolution of dosage compensation 由 Willem Rens, Margaret S. Wallduck, F.L. Lovell, M.A. Ferguson‐Smith, Anne C. Ferguson‐Smith

    出版 2010
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  12. 12
    Chromosome Breakage and Ultrasound

    Chromosome Breakage and Ultrasound 由 E. Boyd, U. Abdulla, Ian Donald, J. E. E. Fleming, A. J. Hall, M.A. Ferguson‐Smith

    出版 1971
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  13. 13
    Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization.

    Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. 由 S Malcolm, Paul J.R. Barton, Clifton N. Murphy, M.A. Ferguson‐Smith, David L. Bentley, Terence H. Rabbitts

    出版 1982
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  14. 14
    Resolution and evolution of the duck-billed platypus karyotype with an X <sub>1</sub> Y <sub>1</sub> X <sub>2</sub> Y <sub>2</sub> X <sub>3</sub> Y <sub>3</sub> X <sub>4</sub> Y <sub>4</sub> X <sub>5</sub> Y <sub>5</sub> male sex chromosome constitution

    Resolution and evolution of the duck-billed platypus karyotype with an X <sub>1</sub> Y <sub>1</sub> X <sub>2</sub> Y <sub>2</sub> X <sub>3</sub> Y <sub>3</sub> X <sub>4</sub> Y <s... 由 Willem Rens, Frank Grützner, Patrícia C. M. O’Brien, Helen Fairclough, Jennifer A. Marshall Graves, M.A. Ferguson‐Smith

    出版 2004
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  15. 15
    Variable transfer of Y-specific sequences in XX males

    Variable transfer of Y-specific sequences in XX males 由 Nabeel A. Affara, M.A. Ferguson‐Smith, John Tolmie, KY Kwok, Michael Mitchell, Derek J. Jamieson, April Cook, L. Florentin

    出版 1986
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  16. 16
    Clinical Features and Natural History of von Hippel-Lindau Disease

    Clinical Features and Natural History of von Hippel-Lindau Disease 由 Eamonn R. Maher, John R.W. Yates, R W J Harries, Caroline Benjamin, R Harris, Anthony T. Moore, M.A. Ferguson‐Smith

    出版 1990
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  17. 17
    Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)

    Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency) 由 Elizabeth F. Gillard, Nabeel A. Affara, John R.W. Yates, David Goudie, J. C. Lambert, D.A. Aitken, M.A. Ferguson‐Smith

    出版 1987
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  18. 18
    Comparative analysis of sex chromosomes in Leporinus species (Teleostei, Characiformes) using chromosome painting

    Comparative analysis of sex chromosomes in Leporinus species (Teleostei, Characiformes) using chromosome painting 由 Patrícia Parise-Maltempi, Edson Lourenço da Silva, Willem Rens, Frances L. Dearden, Patricia C. O’Brien, Vladimir A. Trifonov, M.A. Ferguson‐Smith

    出版 2013
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  19. 19
    Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.

    Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting. 由 Yaru Zheng, N P Carter, Cathy M. Price, S M Colman, P. J. D. Milton, GeraldA Hackett, M. F. Greaves, M.A. Ferguson‐Smith

    出版 1993
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  20. 20
    Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

    Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. 由 Nigel P. Carter, M.A. Ferguson‐Smith, M T Perryman, H. Telenius, Adele Pelmear, M. Leversha, Mary Glancy, Stephen Wood, K Cook, H M Dyson

    出版 1992
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