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Results: 1-9 |
Results: 9
REDUCTION OF PLATELET SEPARATION TIME - EVALUATION OF A NEW SOFTWARE VERSION
Authors: SCHUNTERMANN I BRAND G GRUNENBERG R GATHOF BS
Citation: I. Schuntermann et al., REDUCTION OF PLATELET SEPARATION TIME - EVALUATION OF A NEW SOFTWARE VERSION, Transfusion, 38(10), 1998, pp. 16-16
NOVEL INITIATION CODON MUTATION MET1THR IDENTIFIED IN A PATIENT WITH PARTIAL HYPOXANTHINE-GUANINE PHOSPHORIBOSYL-TRANSFERASE (HPRT) DEFICIENCY - HPRT HEIDELBERG
Authors: GATHOF BS GEISSLER J WINGEN AM GRESSER U
Citation: Bs. Gathof et al., NOVEL INITIATION CODON MUTATION MET1THR IDENTIFIED IN A PATIENT WITH PARTIAL HYPOXANTHINE-GUANINE PHOSPHORIBOSYL-TRANSFERASE (HPRT) DEFICIENCY - HPRT HEIDELBERG, Human mutation, 7(2), 1996, pp. 184-184
CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION (VOL 96, PG 721, 1995)
Authors: GATHOF BS SOMMER M PODSKARBI T REICHARDT J BRAUN A GRESSER U SHIN YS
Citation: Bs. Gathof et al., CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION (VOL 96, PG 721, 1995), Human genetics, 97(5), 1996, pp. 699-699
3 MISSENSE MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 FAMILIES WITH MILD GALACTOSEMIA
Authors: SHIN YS GATHOF BS PODSKARBI T SOMMER M GIUGLIANI R GRESSER U
Citation: Ys. Shin et al., 3 MISSENSE MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 FAMILIES WITH MILD GALACTOSEMIA, European journal of pediatrics, 155(5), 1996, pp. 393-397
MOLECULAR CHARACTERIZATION OF DUARTE-1 AND DUARTE-2 VARIANTS OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE
Authors: PODSKARBI T KOHLMETZ T GATHOF BS KLEINLEIN B BIEGER WP GRESSER U SHIN YS
Citation: T. Podskarbi et al., MOLECULAR CHARACTERIZATION OF DUARTE-1 AND DUARTE-2 VARIANTS OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE, Journal of inherited metabolic disease, 19(5), 1996, pp. 638-644
CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION
Authors: GATHOF BS SOMMER M PODSKARBI T REICHARDT J BRAUN A GRESSER U SHIN YS
Citation: Bs. Gathof et al., CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION, Human genetics, 96(6), 1995, pp. 721-725
CAPILLARY ELECTROPHORESIS FOR SCREENING OF ADENYLOSUCCINATE LYASE DEFICIENCY
Authors: GROSS M GATHOF BS KOLLE P GRESSER U
Citation: M. Gross et al., CAPILLARY ELECTROPHORESIS FOR SCREENING OF ADENYLOSUCCINATE LYASE DEFICIENCY, Electrophoresis, 16(10), 1995, pp. 1927-1929
MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 2 FAMILIES WITH MILD GALACTOSEMIA VARIANTS
Authors: SOMMER M GATHOF BS PODSKARBI T GIUGLIANI R KLEINLEIN B SHIN YS
Citation: M. Sommer et al., MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 2 FAMILIES WITH MILD GALACTOSEMIA VARIANTS, Journal of inherited metabolic disease, 18(5), 1995, pp. 567-576
PARTIAL HGPRT-DEFICIENCY, PHEOCHROMOCYTOMA AND ERYTHROCYTOSIS
Authors: KAMILLI I GRESSER U GATHOF BS GROBNER W
Citation: I. Kamilli et al., PARTIAL HGPRT-DEFICIENCY, PHEOCHROMOCYTOMA AND ERYTHROCYTOSIS, Journal of inherited metabolic disease, 16(2), 1993, pp. 484-485
Risultati: 1-9 |