L. Stolpe

394delTT: a Nordic cystic fibrosis mutation

M. Schwartz, M. Claustres, M. Anvret, 1994, Human Genetics.

Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families

M. Starborg, M. Anvret, M. Nordenskjöld, 1991, Clinical genetics.

The Trophoblastic Epithelial Barrier Is Not Infected in Full-Term Placentae of Human Immunodeficiency Virus-Seropositive Mothers Undergoing Antiretroviral Therapy

J. Albert, E. Fenyö, M. Anvret, 1999, Journal of Virology.

Frequency of four cystic fibrosis mutations in a Swedish population

B. Strandvik, U. Gyllensten, M. Allen, 1993, Acta paediatrica.

A normal male with an inherited deletion of one exon within the DMD gene

L. Edström, M. Anvret, M. Nordenskjöld, 2004, Human Genetics.

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the “critical segment” towards the telomere

M. Anvret, M. Nordenskjöld, L. Johansson, 1991, Human Genetics.