Practical Genetic Counselling

Por MacLeod, P.M.
Publicado em 1982

Forget cloning sheep and pay attention to China

Por MacLeod, P, Fraser, C
Publicado em 1998

Accutane-induced teratogenesis

Por Robertson, R., MacLeod, P.M.
Publicado em 1985

Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant

Por MacLeod, P., Mackenzie, S., Scriver, C. R.
Publicado em 1972

Cloning in Escherichia coli K-12 of a Na+-dependent transport system from a marine bacterium.

Por MacLeod, P R, MacLeod, R A
Publicado em 1986

Spontaneous subcutaneous and mediastinal emphysema--a complication of lung function tests in Pneumocystis carinii pneumonia.

Por Ramakrishnan, S., MacLeod, P. M., Tyrell, C. J.
Publicado em 1988

Fine structure of cutaneous nerves in ganglioside storage disease.

Por Dolman, C L, MacLeod, P M, Chang, E
Publicado em 1977

Gaucher disease: molecular screening of the glucocerebrosidase 1601G and 1601A alleles in Victoria, British Columbia, Canada.

Por Choy, F Y, Linsey, J, MacLeod, P D
Publicado em 1997

Growth hormone response in fetal alcohol syndrome.

Por Tze, W J, Friesen, H G, MacLeod, P M
Publicado em 1976

Letter: Slide test for alpha-fetoprotein.

Por Baird, P. A., Applegarth, D. A., Lowry, R. B., Miller, J. R., MacLeod, P. M.
Publicado em 1976

Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2

Por Saxena, A, de Lagarde, D, Leonard, H, Williamson, S L, Vasudevan, V, Christodoulou, J, Thompson, E, MacLeod, P, Ravine, D
Publicado em 2006

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Por Drumheller, T, McGillivray, B C, Behrner, D, MacLeod, P, McFadden, D E, Roberson, J, Venditti, C, Chorney, K, Chorney, M, Smith, D I
Publicado em 1996

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Por Lynch, E D, Ostermeyer, E A, Lee, M K, Arena, J F, Ji, H, Dann, J, Swisshelm, K, Suchard, D, MacLeod, P M, Kvinnsland, S, Gjertsen, B T, Heimdal, K, Lubs, H, Møller, P, King, M C
Publicado em 1997

Familial gastric cancer: overview and guidelines for management*

Por Caldas, C., Carneiro, F., Lynch, H., Yokota, J., Wiesner, G., Powell, S., Lewis, F., Huntsman, D., Pharoah, P., Jankowski, J., MacLeod, P., Vogelsang, H., Keller, G., Park, K., Richards, F., Maher, E., Gayther, S., Oliveira, C., Grehan, N., Wight, D., Seruca, R., Roviello, F., Ponder, B., Jackson, C.
Publicado em 1999

Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria

Por Brooks-Wilson, A, Kaurah, P, Suriano, G, Leach, S, Senz, J, Grehan, N, Butterfield, Y, Jeyes, J, Schinas, J, Bacani, J, Kelsey, M, Ferreira, P, MacGillivray, B, MacLeod, P, Micek, M, Ford, J, Foulkes, W, Australie, K, Greenberg, C, LaPointe, M, Gilpin, C, Nikkel, S, Gilchrist, D, Hughes, R, Jackson, C, Monaghan, K, Oliveira, M, Seruca, R, Gallinger, S, Caldas, C, Huntsman, D
Publicado em 2004

Proceed with Care: Direct Predictive Testing for Huntington Disease

Por Benjamin, C. M., Adam, S., Wiggins, S., Theilmann, J. L., Copley, T. T., Bloch, M., Squitieri, F., McKellin, W., Cox, S., Brown, S. A., Kremer, H. P. H., Burgess, M., Meshino, W., Summers, A., Macgregor, D., Buchanan, J., Greenberg, C., Carson, N., Ives, E., Frecker, M., Welch, J. P., Fuller, A., Rosenblatt, D., Miller, S., Dufrasne, S., Roy, M., Andermann, E., Prevost, C., Khalifa, M., Girard, K., Taylor, S., Hunter, A., Goldsmith, C., Whelan, D., Eisenberg, D., Soltan, H., Kane, J., Shokeir, M. H. K., Gibson, A., Cardwell, S., Bamforth, S., Grover, S., Suchowersky, O., Klimek, M., Garber, T., Gardner, H. A., MacLeod, P., Hayden, M. R.
Publicado em 1994