2023 - Research.com Genetics in United Kingdom Leader Award
1989 - Member of Academia Europaea
1988 - Polish Academy of Science
1983 - Fellow of the Royal Society, United Kingdom
1978 - Fellow of the Royal Society of Edinburgh
Genetics, Karyotype, Chromosome, Molecular biology and Y chromosome are his primary areas of study. His study in Gene, X chromosome, Genome, Chromosome 21 and Chromosome 22 is done as part of Genetics. His studies deal with areas such as Metaphase, Hybridization probe, Phylogenetic tree, Chromosomal translocation and Fluorescence in situ hybridization as well as Karyotype.
He usually deals with Chromosome and limits it to topics linked to Human genetics and Chromosome painting. The study incorporates disciplines such as Chromosome microdissection, Locus and Cytogenetics in addition to Molecular biology. The concepts of his Y chromosome study are interwoven with issues in Chromosome 4 and Phylogenetics.
His primary areas of investigation include Genetics, Karyotype, Chromosome, Evolutionary biology and Molecular biology. Gene, Gene mapping, X chromosome, Locus and Genome are among the areas of Genetics where Malcolm A. Ferguson-Smith concentrates his study. His Karyotype study incorporates themes from Zoology, Ploidy, Phylogenetic tree and Cytogenetics.
Malcolm A. Ferguson-Smith has researched Chromosome in several fields, including Homologous chromosome and Chromosomal translocation. His Evolutionary biology research is multidisciplinary, incorporating elements of Leucopternis albicollis, Chromosome painting and Phylogenetics. In his research on the topic of Molecular biology, Chromosome 19 is strongly related with Chromosome 21.
Malcolm A. Ferguson-Smith mainly investigates Evolutionary biology, Karyotype, Chromosome, Genetics and Microchromosome. His Evolutionary biology study combines topics in areas such as Leucopternis albicollis, Chromosome painting, Species complex, Phylogenetic tree and Hylaeamys megacephalus. The Karyotype study combines topics in areas such as Phylogenetics, Ploidy and Cytogenetics.
His Chromosome research also works with subjects such as
His primary areas of study are Karyotype, Evolutionary biology, Chromosome, Genetics and Microchromosome. His study with Karyotype involves better knowledge in Gene. His Evolutionary biology research includes themes of Species complex, Phylogenetic tree, Hylaeamys megacephalus, Oryzomyini and Centromere.
His biological study spans a wide range of topics, including Homologous chromosome, Salamander and Chromosomal translocation. Malcolm A. Ferguson-Smith integrates several fields in his works, including Genetics and Context. His Microchromosome study combines topics from a wide range of disciplines, such as DNA sequencing and Anolis.
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Multicolor Spectral Karyotyping of Human Chromosomes
E. Schröck;S. du Manoir;T. Veldman;B. Schoell.
Science (1996)
Clinical Features and Natural History of von Hippel-Lindau Disease
E R Maher;J R Yates;R Harries;Caroline Benjamin.
QJM: An International Journal of Medicine (1990)
Translocation of c- abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia
Claus R. Bartram;Annelies de Klein;Anne Hagemeijer;Ton van Agthoven.
Nature (1983)
Genome analysis of the platypus reveals unique signatures of evolution
Wesley C. Warren;La Deana W. Hillier;Jennifer A. Marshall Graves;Ewan Birney.
Nature (2008)
Cytogenetic analysis by chromosome painting using dop-pcr amplified flow-sorted chromosomes
H Telenius;A H Pelmear;A Tunnacliffe;N P Carter.
Genes, Chromosomes and Cancer (1992)
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
Malcolm A. Ferguson-Smith.
Journal of Medical Genetics (1965)
Von Hippel-Lindau disease: a genetic study.
E R Maher;L Iselius;J R Yates;M Littler.
Journal of Medical Genetics (1991)
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
Berton Zbar;Takeshi Kishida;Fan Chen;Laura Schmidt.
Human Mutation (1996)
Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses
M. A. Ferguson-Smith;J. R. W. Yates.
Prenatal Diagnosis (1984)
X-Y CHROMOSOMAL INTERCHANGE IN THE ÆTIOLOGY OF TRUE HERMAPHRODITISM AND OF XX KLINEFELTER'S SYNDROME
M.A. Ferguson-Smith.
The Lancet (1966)
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