Concepedia

Refik Özcan

RÖ

3

Publications

307

Citations

3

H-Index

1996

Active since

Affiliations

Boston Children's Hospital(Current)

Universitätskinderklinik

Harvard University

Refik Özcan is an author at Boston Children's Hospital specializing in genetics, molecular genetics, and medicine.

Top concepts

Publications per year

1996–2003

3

Publications

3

Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Stefan Eber, Jennifer M. Reingle González, Marcia L. Lux et al. · Nature Genetics · 1996 · 216 citations

, , +7

Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.

Y Yawata, A Kanzaki, Ayumi Yawata et al. · PubMed · 2000 · 76 citations

Simultaneous (AC)<sub>n</sub> microsatellite polymorphism analysis and single‐stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin‐1 mutations in dominant hereditary spherocytosis

Refik Özcan, Petr Jarolı́m, Samuel E. Lux et al. · British Journal of Haematology · 2003 · 15 citations · Full text

, , +18

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