M. Magnusson

Variability in the Michelin tire syndrome. A child with multiple anomalies, smooth muscle hamartoma, and familial paracentric inversion of chromosome 7q.

E. Zackai, N. Spinner, R. Schnur, 1993, Journal of the American Academy of Dermatology.

Deep Venous Thrombosis of the Lower Limb: No Difference in Duration of Symptoms Between Proximal and Distal Disease

F. Labruto, M. Westerberg, M. Magnusson, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrences.

I. Krantz, L. Jukofsky, J. Ming, 2001, American journal of medical genetics.

Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.

J. Kere, B. Andersen, I. Fransson, 2014, American journal of human genetics.

Lateral meningocele syndrome: three new patients and review of the literature.

E. Zackai, A. Duhaime, S. Zderic, 1997, American journal of medical genetics.

Association and Mutation Analyses of the IRF6 Gene in Families with Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate

J. Kere, I. Fransson, P. Unneberg, 2014, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.