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Praxis|June 5, 2001
[Chronic progressive polycythemia and thrombocytosis]R Forkert, Y Ko, S Fronhoffs, et al.
Neuropediatrics|February 1, 1996
Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findingsS Rudnik-Schöneborn, R Forkert, E Hahnen, et al.
Human Molecular Genetics|October 1, 1995
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individualsE Hahnen, R Forkert, C Marke, et al.
Annals of Hematology|April 29, 2018
Consensus statement for cancer patients requiring intensive care supportM G Kiehl, G Beutel, B Böll, et al.
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