Practical Genetic Counselling

par MacLeod, P.M.
Publié 1982

Forget cloning sheep and pay attention to China

par MacLeod, P, Fraser, C
Publié 1998

Accutane-induced teratogenesis

par Robertson, R., MacLeod, P.M.
Publié 1985

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

par MacLeod, P., Mackenzie, S., Scriver, C. R.
Publié 1972

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

par MacLeod, P R, MacLeod, R A
Publié 1986

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

par Ramakrishnan, S., MacLeod, P. M., Tyrell, C. J.
Publié 1988

Fine structure of cutaneous nerves in ganglioside storage disease.

par Dolman, C L, MacLeod, P M, Chang, E
Publié 1977

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

par Choy, F Y, Linsey, J, MacLeod, P D
Publié 1997

Growth hormone response in fetal alcohol syndrome.

par Tze, W J, Friesen, H G, MacLeod, P M
Publié 1976

Letter: Slide test for alpha-fetoprotein.

par Baird, P. A., Applegarth, D. A., Lowry, R. B., Miller, J. R., MacLeod, P. M.
Publié 1976

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

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

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

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

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

par 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
Publié 1997

Familial gastric cancer: overview and guidelines for management*

par 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.
Publié 1999

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

par 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
Publié 2004

Proceed with Care: Direct Predictive Testing for Huntington Disease

par 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.
Publié 1994