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Name: Iain R. McIntosh, PhD
Research Division: The Johns Hopkins University, Medical Genetics
City, State: Baltimore, MD
Phone: (410) 955-7948
Fax: (410) 614-2522
URL: http://www.med.jhu.edu/nps/index.html
E-mail: imcintos@jhmi.edu

Title: Assistant Professor
Academic
Appointments:
Assistant Professor of Medicine
Degree(s): B.Sc. in Biological Sciences (with Upper 2nd Class Honours in Genetics), 1984, University of Edinburgh
Ph.D. in Genetics, 1988, University of Edinburgh
Research
Interests:
Molecular genetics of Nail Patella Syndrome; Genetics basis of facial clefting; Gene expression in development

References:

Wyszynski, D.F., Maestri, N., Lewanda, A.F., McIntosh, I., Smith, E.A., Garcia-Delgado, C., Vinageras-Guarneros, E., Wulfsberg, E., and Beaty, T.H.
No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populations.
Hum Hered 47(2):101-109, 1997
abstract

Wyszynski, D.F., Maestri, N., McIntosh, I., Smith, E.A., Lewanda, A.F., Garcia-Delgado, C., Vinageras-Guarneros, E., Wulfsberg, E., and Beaty, T.H.
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families.
Hum Genet 99(1): 22-26, 1997
abstract

Maestri, N.E., Beaty, T.H., Hetmanski, J., Smith, E.A., McIntosh, I., Wyszynski, D.F., Liang, K.Y., Duffy, D.L., and Vander Kolk, C.
Application of transmission disequilibrium tests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the models.
Am J Med Genet 73(3): 337-344, 1997
abstract

McIntosh, I., Dreyer, S.D., Clough, M.V., Dunston, J.A., Eyaid, W., Roig, C.M., Montgomery, T., Ala-Mello, S., Kitila, I., Winterpacht, A., Zabel, B., Frydman, M., Cole, W.G., Francomano, C.A., and Lee, B.
Mutation analysis of LMX1B gene in nail-patella syndrome patients.
Am J Hum Genet 63(6): 1651-1658, 1998
abstract

Vollrath, D., Jaramillo-Babb, V.L., Clough, M.V., McIntosh, I., Scott, K.M., Lichter, P.R., and Richards, J.E.
Loss-of-function mutations in the LIM- homeodomain gene, LMX1B, in nail-patella syndrome.
Hum. Mol. Genet. 7: 1091-1098, 1998
abstract

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Last Updated: 11/15/01

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