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Wendy McKinnon

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Jeffrey W Innis; Frances R Goodman; Chiara Bacchelli; Thomas M Williams; Douglas P Mortlock; Praveen Sateesh; Peter J Scambler; Wendy McKinnon; Alan E Guttmacher
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.
A Bourdeau; Urszula Cymerman; M E Paquet; W Meschino; Wendy McKinnon; A E Guttmacher; L Becker; Michelle Letarte
Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1.
T D Taylor; Susan J Hayflick; Wendy McKinnon; Alan E Guttmacher; A Hovnanian; M Litt; Jonathan (Jon) Zonana
Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutations.

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2002: Jeffrey W Innis; Frances R Goodman; Chiara Bacchelli; Thomas M Williams; Douglas P Mortlock; Praveen Sateesh; Peter J Scambler; Wendy McKinnon; Alan E Guttmacher
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.
Human mutation 2002;19(5):573-4.
2000: A Bourdeau; Urszula Cymerman; M E Paquet; W Meschino; Wendy McKinnon; A E Guttmacher; L Becker; Michelle Letarte
Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1.
The American journal of pathology 2000;156(3):911-23.
1998: T D Taylor; Susan J Hayflick; Wendy McKinnon; Alan E Guttmacher; A Hovnanian; M Litt; Jonathan (Jon) Zonana
Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutations.
The Journal of investigative dermatology 1998;111(1):83-5.
1997: Timothy Howard; Alan E Guttmacher; Wendy McKinnon; M Sharma; Victor A McKusick; Ethylin Jabs
Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus.
American journal of human genetics 1997;61(6):1405-12.
1996: Susan J Hayflick; T Taylor; Wendy McKinnon; Alan E Guttmacher; M Litt; Jonathan (Jon) Zonana
Clouston syndrome (hidrotic ectodermal dysplasia) is not linked to keratin gene clusters on chromosomes 12 and 17.
The Journal of investigative dermatology 1996;107(1):11-4.
1994: K A McAllister; K M Grogg; D W Johnson; Carol J Gallione; M A Baldwin; Charles E Jackson; E A Helmbold; Dorene S Markel; Wendy McKinnon; J Murrell
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.
Nature genetics 1994;8(4):345-51.
1994: K A McAllister; F Lennon; B Bowles-Biesecker; Wendy McKinnon; E A Helmbold; Dorene S Markel; Charles E Jackson; Alan E Guttmacher; Margaret Pericak-Vance; Douglas A Marchuk
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.
Journal of medical genetics 1994;31(12):927-32.
1994: Alan E Guttmacher; Wendy McKinnon; M D Upton
Hereditary hemorrhagic telangiectasia: a disorder in search of the genetics community.
American journal of medical genetics 1994;52(2):252-3.
1994: M T McDonald; K A Papenberg; S Ghosh; A A Glatfelter; Barbara Bowles Biesecker; E A Helmbold; Dorene S Markel; Adam J Zolotor; Wendy McKinnon; J L Vanderstoep
A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34.
Nature genetics 1994;6(2):197-204.