P. Teague

发表

V. Sheffield, A. Cideciyan, S. Jacobson, 2000, American journal of human genetics.

Influences of chromosome size, gene density and nuclear position on the frequency of constitutional translocations in the human population

W. Bickmore, P. Teague, 2004, Chromosome Research.

Differences in the Localization and Morphology of Chromosomes in the Human Nucleus

Peter Teague, Paul Perry, J. A. Croft, 1999, The Journal of cell biology.

Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.

G. Spowart, K. Dry, A. Carothers, 1994, American journal of human genetics.

SALIVARY TESTOSTERONE LEVELS AND THE PROGRESS OF PUBERTY IN THE NORMAL BOY

R. Walker, P. Teague, D. Riad-fahmy, 1989, Clinical endocrinology.

Psychiatric disorder and cognitive function in a family with an inherited novel mutation of the developmental control gene PAX6.

A. Taylor, E. Simonoff, I. Heyman, 1999, Psychiatric genetics.

Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illness

W. Muir, A. Maclean, D. Porteous, 1996, Psychiatric genetics.

Mice with Y chromosome deletion and reduced Rbm genes on a heterozygous Dazl1 null background mimic a human azoospermic factor phenotype.

P. Teague, H. Cooke, R. Speed, 1999, Human reproduction.

Edinburgh Research Explorer Increased level of linkage disequilibrium in rural compared with urban communities

N. Hastie, A. Wright, C. Hayward, 2018 .

Expression profiling of the developing testis in wild‐type and Dazl knockout mice

Peter Teague, Thorsten Forster, Douglas Roy, 2004, Molecular reproduction and development.

Edinburgh study of growth and development of children with sex chromosome abnormalities. III.

P. Teague, S. Ratcliffe, L. Murray, 1979, Birth defects original article series.

Clinical and Genetic Analysis of a Large North European Caucasian Family Affected by Early-onset Periodontitis

P. Teague, D. Kinane, A. Wright, 2000, Journal of dental research.

European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families

J. Weissenbach, H. Cann, R. Vossen, 1996, Annals of human genetics.

Estimating Human Inbreeding Coefficients: Comparison of Genealogical and Marker Heterozygosity Approaches

J. Weber, N. Hastie, I. Rudan, 2006, Annals of human genetics.

Cell proliferation in the developing wing-bud of normal and talpid3 mutant chick embryos.

D. A. Ede, O. Flint, P. Teague, 1975, Journal of embryology and experimental morphology.

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

M Jay, N. Tommerup, E. Bruford, 1997, Genomics.

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

H. J. Evans, M. Jay, S. Bhattacharya, 1994, American journal of human genetics.

Linkage analysis in X-linked congenital stationary night blindness.

K. Dry, M. Jay, P. Teague, 1992, Genomics.

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

A. Bird, M. Jay, A. Wright, 1994, Journal of medical genetics.

A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families

P. Allan, A. Wright, A. Carothers, 2004, Human Genetics.

The genomic organisation of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia

D. Blackwood, W. Muir, D. Porteous, 2001, Molecular Psychiatry.

Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design.

N. Hastie, A. Wright, C. Hayward, 2005, American journal of human genetics.

Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder

D. Blackwood, W. Muir, D. Porteous, 2001, Psychiatric genetics.

Genetic Analysis ofaKindred withX-linked MentalHandicap and Retinitis Pigmentosa

A. Fielder, G. Spowart, K. Dry, 1994 .

Presence of Multiple Functional Polyadenylation Signals and a Single Nucleotide Polymorphism in the 3′ Untranslated Region of the Human Serotonin Transporter Gene

D. Blackwood, W. Muir, A. Ogilvie, 1999, Journal of neurochemistry.

Genetic Studies in Autosomal Recessive Forms of Retinitis Pigmentosa

E. Bruford, M. Patton, M. Jay, 1995 .

Lung Pathology in Response to Repeated Exposure to Staphylococcus aureus in Congenic Residual Function Cystic Fibrosis Mice Does Not Increase in Response to Decreased CFTR Levels or Increased Bacterial Load

D. Davidson, J. Dorin, P. Teague, 2004, Pathobiology.

Heterogeneity Analysis in40X-LinkedRetinitis Pigmentosa Families

M. Jay, M. Dempster, A. Carothers, 1994 .