Browse by all authors Browse By Author Name - Mowat,+D.

Browse Results (2 results found)

Subscribe to the RSS feed for this result setSubscribe to the RSS feed for this result set

  Abstract Views File Downloads Thomson Reuters Web of Science Citation Count Scopus Citation Count Altmetric Score
Roscioli T., Elakis G., Cox T.C., Moon D.J., Venselaar H., Turner A.M., Le T., Hackett E., Haan E., Colley A., Mowat D., Worgan L., Kirk E.P., Sachdev R., Thompson E., Gabbett M., Mcgaughran J., Gibson K., Gattas M., Freckmann M.-L., Dixon J., Hoefsloot L., Field M., Hackett A., Kamien B., Edwards M., Ades L.C., Collins F.A., Wilson M.J., Savarirayan R., Tan T.Y., Amor D.J., Mcgillivray G., White S.M., Glass I.A., David D.J., Anderson P.J., Gianoutsos M. and Buckley M.F. (2013) Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 australian and new zealand patients. American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 163 4: 259-270. doi:10.1002/ajmg.c.31378 21 2 3 Cited 4 times in Scopus4 2
Hämäläinen, R. H., Mowat, D., Gabbett, M. T., O'Brien, T. A., Kallijärvi, J. and Lehesjoki, A. E. (2006) Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism. Clinical Genetics, 70 6: 473-479. doi:10.1111/j.1399-0004.2006.00700.x 49   6 Cited 8 times in Scopus8 3