K. Wieland

发表

The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene.

M. Vidaud, U. Martinowitz, D. Millar, 1990, Blood.

Diagnosis of haemophilia B using the polymerase chain reaction

J. Reiss, B. Zoll, K. Wieland, 2005, Blut.

Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIII.

D. Cooper, V. Kakkar, U. Martinowitz, 1990, Thrombosis research.

A molecular genetic study of factor XI deficiency.

D. Cooper, J. Hancock, V. Kakkar, 1991, Blood.

The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene

D. Cooper, M. Krawczak, D. Whitmore, 1990, Human Genetics.

Application of PCR to the detection and analysis of point mutations in the human factor VIII gene

D. Cooper, V. Kakkar, E. Tuddenham, 1991 .

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Katherine M. Tucker, Sebastian A. Wagner, Kelly J. Sullivan, 2019, Human Mutation.

Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism

D. Cooper, V. Kakkar, D. Millar, 2004, Human Genetics.

Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA

D. Cooper, V. Kakkar, J. Reiss, 1990, Human Genetics.

Combined factor VIII/factor XI deficiency may cause intra‐familial clinical variability in haemophilia A among Ashkenazi Jews

D. Cooper, V. Kakkar, U. Martinowitz, 1994, Blood Coagulation and Fibrinolysis.

HerediCaRe: Dokumentations- und IT-Lösung eines spezialisierten Registers für erblichen Brust- und Eierstockkrebs

R. Schmutzler, C. Engel, E. Hahnen, 2021, Das Gesundheitswesen.