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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.Archives of Andrology|November 7, 2001
Absence of Yq microdeletions in infertile menA Tzschach, B Thamm, B Imthurn, 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.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.Journal of Neurology|February 1, 1989
Clinico-neurological investigations in the fra(X) form of mental retardationP Vieregge, U Froster-IskeniusClinical Dysmorphology|January 1, 1992
Encephalocele, radial defects, cardiac, gastrointestinal, anal, and renal anomalies: a new multiple congenital anomaly (MCA) syndrome?U Froster-Iskenius, P MeineckeEuropean Journal of Pediatrics|May 1, 1985
Caudal dysplasia and femoral hypoplasia-unusual facies syndrome: different manifestations of the same disorder?F Riedel, U Froster-IskeniusCasopis Lekaru Ceskych|November 26, 2003
[Methods of determination of the number of CTG/CAG repeats in trinucleotide repeats in the human genome]M Falk, U Froster, M VojtískováHuman Genetics|January 1, 1984
Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large familiesU Froster-Iskenius, A Schulze, E SchwingerMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1989
[Knee pterygium syndrome in a newborn infant]P Meinecke, J Menzel, U Froster-IskeniusPageof 7