Concepedia

Mikael Lindlöf

ML

15

Publications

1.5K

Citations

14

H-Index

1985

Active since

Affiliations

University of Helsinki(Current)

Väestöliitto

Baylor Genetics

Inserm

University of Würzburg

Mikael Lindlöf is an author at University of Helsinki specializing in medicine, molecular genetics, and genetics.

Top concepts

Publications per year

1985–2011

15

Publications

15

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf et al. · PubMed · 1989 · 961 citations

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

Albert de la Chapelle, Eeva‐Marja Sankila, Mikael Lindlöf et al. · Clinical Genetics · 1985 · 77 citations

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Gene deletions in X-linked muscular dystrophy.

Mikael Lindlöf, A Kiuru, H Kääriäinen et al. · PubMed · 1989 · 74 citations

Erythropoietin Receptor Mutations Associated With Familial Erythrocytosis Cause Hypersensitivity to Erythropoietin in the Heterozygous State

Stephanie S. Watowich, Xiaoling Xie, Ursula Klingmüller et al. · Blood · 1999 · 57 citations

Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Study of Comprehension of the Test Results and Social and Psychological Significance of the Testing

Outi Järvinen, Anna‐Elina Lehesjoki, Mikael Lindlöf et al. · PEDIATRICS · 2000 · 53 citations

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