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E. Kleihauer

University of Ulm

85

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2100

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Thalassemia intermedia: compound heterozygous beta zero/beta(+)-thalassemia and co-inherited heterozygous alpha(+)-thalassemia.

1993 Annals of Hematology
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A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia

1992 Blood
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The spectrum of CFTR mutations in south-west German cystic fibrosis patients

1992 Human Genetics
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A Deletion/Inversion Rearrangement of the β-Globin Gene Cluster in a Turkish Family With δβ°-Thalassemia Intermedia

1992 Blood
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ConvenientScreeningfor Hemoglobin Variantsby Usingthe DiamatHPLCSystem

1990
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Clonal Analysis of Myelodysplastic Syndromes: Evidence of Multipotent Stem Cell Origin

1989 Blood
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HLA-haploidentical bone marrow transplantation in three infants with adenosine deaminase deficiency: Stable immunological reconstitution and reversal of skeletal abnormalities

1989 European Journal of Pediatrics
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Die molekulare Grundlage der hereditären Persistenz fetalen Hämoglobins (HPFH) und des Hämoglobinschaltmechanismus: Ein Beitrag zur klinischen Bedeutung unter besonderer Berücksichtigung der Corfu-δβo-Thalassämie

1988 Monatsschrift Kinderheilkunde
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Rapid and non‐radioactive prenatal diagnosis of β thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)

1988 British Journal of Haematology
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The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia

1988 Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft für Kinderheilkunde
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