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Kinderarztliche Praxis|October 1, 1993
[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication]H Reichenbach, H Holland, B Thamm, et al.Der Anaesthesist|April 11, 2000
[In vitro contracture test and gene typing in diagnosing malignant hyperthermia. Each as an appropriate complement to the other method]H Rüffert, D Olthoff, C Deutrich, et al.British Journal of Anaesthesia|August 9, 2001
Homozygous and heterozygous Arg614Cys mutations (1840C-->T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German familyH Rueffert, D Olthoff, C Deutrich, et al.FEBS Letters|September 17, 1998
Use of the phage display technique for detection of epitopes recognized by polyclonal rabbit gliadin antibodiesA A Osman, H Uhlig, B Thamm, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|May 18, 2004
Applicability of the SHBG androgen sensitivity test in the differential diagnosis of 46,XY gonadal dysgenesis, true hermaphroditism, and androgen insensitivity syndromeA Krause, G H G Sinnecker, O Hiort, et al.Archives of Andrology|November 7, 2001
Absence of Yq microdeletions in infertile menA Tzschach, B Thamm, B Imthurn, et al.Prenatal Diagnosis|March 12, 1999
Pitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin geneS Vondran, J Edelmann, H Holland, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|May 14, 2005
Gonadoblastomas in 5 patients with 46,XY gonadal dysgenesisW Hoepffner, L-C Horn, E Simon, et al.Zeitschrift Fur Kardiologie|August 25, 2000
[Late diagnosis of Curschmann-Steinert myotonic dystrophy in a female patient with dilated cardiomyopathy and in her son]O Gunkel, H Reichenbach, B Thamm, et al.Cancer|October 1, 1995
Molecular and immunohistochemical p53 status in liposarcoma and malignant fibrous histiocytoma: identification of seven new mutations for soft tissue sarcomasH Taubert, P Würl, A Meye, et al.Pageof 2