B. Thamm

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

Thilo Dörk, Milan Maçek, Frauke Mekus et al. · Human Genetics · 2000 · 145 citations

Fibrosis, Mendelian Disorder, Genetic Disorder +11

Molecular and immunohistochemical p53 status in liposarcoma and malignant fibrous histiocytoma. Identification of seven new mutations for soft tissue sarcomas

Helge Täubert, Peter Würl, Axel Meye et al. · Cancer · 1995 · 45 citations · Full text

Use of the phage display technique for detection of epitopes recognized by polyclonal rabbit gliadin antibodies

Awad A. Osman, Holm H. Uhlig, B. Thamm et al. · FEBS Letters · 1998 · 24 citations · Full text

Homozygous and heterozygous Arg614Cys mutations (1840C→T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family

Henrik Rueffert, D Olthoff, C. Deutrich et al. · British Journal of Anaesthesia · 2001 · 20 citations · Full text

Signal Transduction, Molecular Physiology, Genetic Disorder +6

Applicability of the SHBG Androgen Sensitivity Test in the Differential Diagnosis of 46,XY Gonadal Dysgenesis, True Hermaphroditism, and Androgen Insensitivity Syndrome

Alina Krause, Gernot H.G. Sinnecker, Olaf Hiort et al. · Experimental and Clinical Endocrinology & Diabetes · 2004 · 18 citations

Fertility, Genetics, Reproductive Health +20