Ferguson-Smith, M.A. (Malcolm Andrew)
Ferguson-Smith, M.A
Ferguson-Smith, M. A. (1931- ).
Malcolm Ferguson-Smith British geneticist
Ferguson-Smith, Malcolm
Ferguson-Smith, Malcolm Andrew
Ferguson-Smith, Malcolm A.
Ferguson-Smith, Malcolm Andrew, 1931-....
Ferguson-Smith, Malcolm, 1931-
Ferguson-Smith, M. A. (Malcolm Andrew), 1931-
VIAF ID: 101077130 (Personal)
Permalink: http://viaf.org/viaf/101077130
Preferred Forms
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100 1 _ ‡a Ferguson-Smith, M. A.
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100 1 _ ‡a Ferguson-Smith, M. A. ‡q (Malcolm Andrew)
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100 1 _ ‡a Ferguson-Smith, M. A. ‡q (Malcolm Andrew)
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100 1 _ ‡a Ferguson-Smith, Malcolm A.
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100 1 _ ‡a Ferguson-Smith, Malcolm Andrew
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100 1 _ ‡a Ferguson-Smith, Malcolm Andrew, ‡d 1931-....
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100 0 _ ‡a Malcolm Ferguson-Smith ‡c British geneticist
4xx's: Alternate Name Forms (34)
Works
Title | Sources |
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Accidental X-Y recombination and the aetiology of XX males and true hermaphrodites. |
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Amniotic-fluid alpha-fetoprotein in the antenatal diagnosis of spina bifida |
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Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2 |
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The BSE inquiry : return to an order of the Honourable the House of Commons dated October 2000 for the report, evidence and supporting papers of the inquiry into the emergence and identification of bovine spongiform encephalopathy (BSE) and variant Creutzfeldt-Jakob disease (vCJD) and the action taken in response to it up to 20 March 1996 |
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Chromation-positive Klinefelter's syndrome (primary microrchidism) in a mental-deficiency hospital. |
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Chromosomal phylogeny of Vampyressine bats (Chiroptera, Phyllostomidae) with description of two new sex chromosome systems |
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Chromosome homology between chicken (Gallus gallus domesticus) and the red-legged partridge (Alectoris rufa); evidence of the occurrence of a neocentromere during evolution. |
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Chromosome number of the chimpanzee, Pan troglodytes |
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Chromosome painting reveals multiple rearrangements between Gymnotus capanema and Gymnotus carapo (Gymnotidae, Gymnotiformes). |
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Comparative chromosome painting in hummingbirds (Trochilidae) |
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A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps. |
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Cytotaxonomy and Molecular Analyses of Mycteria americana (Ciconiidae: Ciconiiformes): Insights on Stork Phylogeny |
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The emergence of a new sex-system (XX/XY<sub>1</sub>Y<sub>2</sub>) suggests a species complex in the "monotypic" rodent Oecomys auyantepui (Rodentia, Sigmodontinae) |
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Essential medical genetics |
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The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals |
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Evolutionary dynamics of Anolis sex chromosomes revealed by sequencing of flow sorting-derived microchromosome-specific DNA. |
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Extensive Chromosomal Reorganization in the Evolution of New World Muroid Rodents (Cricetidae, Sigmodontinae): Searching for Ancestral Phylogenetic Traits |
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Findings and conclusions |
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FISH with whole chromosome and telomeric probes demonstrates huge karyotypic reorganization with ITS between two species of Oryzomyini (Sigmodontinae, Rodentia): Hylaeamys megacephalus probes on Cerradomys langguthi karyotype. |
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Fundamentos de genética médica |
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A G-->A substitution in an HNF I binding site in the human alpha-fetoprotein gene is associated with hereditary persistence of alpha-fetoprotein (HPAFP). |
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Gender verification in sport: the need for change? |
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Genetyka medyczna |
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Genome analysis of the platypus reveals unique signatures of evolution |
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Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development |
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Hybridization between subterranean tuco-tucos (Rodentia, Ctenomyidae) with contrasting phylogenetic positions |
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Identification of two independent X-autosome translocations in closely related mammalian (Proechimys) species |
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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS |
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Klinefelter's syndrome; frequency and testicular morphology in relation to nuclear sex |
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Leitfaden der Humangenetik |
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Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34. |
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Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. |
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Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes |
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Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses |
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Mechanisms in vertebrate sex determination : a discussion |
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Medicines and cosmetics |
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Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7 |
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Multicolor Spectral Karyotyping of Human Chromosomes |
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Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1. |
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The multiple sex chromosomes of platypus and echidna are not completely identical and several share homology with the avian Z |
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n84133634 |
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Natural selection for genetic variants in sport: the role of Y chromosome genes in elite female athletes with 46,XY DSD. |
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New insights into sex chromosome evolution in anole lizards (Reptilia, Dactyloidae). |
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Observations on the satellited human chromosomes |
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Pachytene analysis in a human reciprocal (10;11) translocation |
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A phylogenetic analysis using multidirectional chromosome painting of three species (Uroderma magnirostrum, U. bilobatum and Artibeus obscurus) of subfamily Stenodermatinae (Chiroptera-Phyllostomidae). |
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Phylogenetic reconstruction by cross-species chromosome painting and G-banding in four species of Phyllostomini tribe (Chiroptera, Phyllostomidae) in the Brazilian Amazon: an independent evidence for monophyly |
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Podstawy genetyki medycznej / J. M. Connor, M. A. Ferguson-Smith. - Warszawa, 1991. |
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Prenat. diagn. (Print) |
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Prenatal chromosome analysis and its impact on the birth incidence of chromosome disorders |
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Prenatal diagnosis and screening |
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Prenatal diagnosis of genetic disorders of the foetus : report |
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Prenatal diagnosis : official journal of Ispd, International society for prenatal diagnosis |
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Primary amentia and micro-orchidism associated with an XXXY sex-chromosome constitution. |
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Reaction to the emergence of BSE in the UK: what was done and what perhaps might have been done better |
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Reciprocal chromosome painting between two South American bats: Carollia brevicauda and Phyllostomus hastatus (Phyllostomidae, Chiroptera). |
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Resolution and evolution of the duck-billed platypus karyotype with an X1Y1X2Y2X3Y3X4Y4X5Y5 male sex chromosome constitution. |
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Responsibilities for human and animal health |
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Saishin idenshi igaku. |
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Sex determination in mouse and man : proceedings of a Royal Society discussion meeting held on 9 and 10 March 1988 |
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THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES |
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A time- and cost-effective strategy to sequence mammalian Y Chromosomes: an application to the de novo assembly of gorilla Y |
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Tolmie collection |
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Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia |
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Turner's Syndrome and phenotype |
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Wakariyasui rinshō idengaku |
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わかりやすい臨床遺伝学 |
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最新遺伝子医学 |
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