AAAAAA

   
Results: 1-8 |
Results: 8
CONGENITAL ERYTHROPOIETIC PORPHYRIA - PROLONGED HIGH-LEVEL EXPRESSIONAND CORRECTION OF THE HEME BIOSYNTHETIC DEFECT BY RETROVIRAL-MEDIATEDGENE-TRANSFER INTO PORPHYRIC AND ERYTHROID-CELLS
Authors: KAUPPINEN R GLASS IA AIZENCANG G ASTRIN KH ATWEH GF DESNICK RJ
Citation: R. Kauppinen et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - PROLONGED HIGH-LEVEL EXPRESSIONAND CORRECTION OF THE HEME BIOSYNTHETIC DEFECT BY RETROVIRAL-MEDIATEDGENE-TRANSFER INTO PORPHYRIC AND ERYTHROID-CELLS, Molecular genetics and metabolism ( Molecular genetics and metabolism (Print)), 65(1), 1998, pp. 10-17
STEROID SULFATASE DEFICIENCY IS THE MAJOR CAUSE OF EXTREMELY LOW ESTRIOL PRODUCTION AT MID-PREGNANCY - A URINARY STEROID ASSAY FOR THE DISCRIMINATION OF STEROID SULFATASE DEFICIENCY FROM OTHER CAUSES
Authors: GLASS IA LAM RC CHANG T ROITMAN E SHAPIRO LJ SHACKLETON CHL
Citation: Ia. Glass et al., STEROID SULFATASE DEFICIENCY IS THE MAJOR CAUSE OF EXTREMELY LOW ESTRIOL PRODUCTION AT MID-PREGNANCY - A URINARY STEROID ASSAY FOR THE DISCRIMINATION OF STEROID SULFATASE DEFICIENCY FROM OTHER CAUSES, Prenatal diagnosis, 18(8), 1998, pp. 789-800
TRISOMY 2Q11.2-]Q21.1 RESULTING FROM AN UNBALANCED INSERTION IN 2 GENERATIONS
Authors: GLASS IA STORMER P OEI PTSP HACKING E COTTER PD
Citation: Ia. Glass et al., TRISOMY 2Q11.2-]Q21.1 RESULTING FROM AN UNBALANCED INSERTION IN 2 GENERATIONS, Journal of Medical Genetics, 35(4), 1998, pp. 319-322
PREVALENCE OF PRO250ARG MUTATION OF FIBROBLAST GROWTH-FACTOR RECEPTOR-3 IN CORONAL CRANIOSYNOSTOSIS
Authors: MOLONEY DM WALL SA ASHWORTH GJ OLDRIDGE M GLASS IA FRANCOMANO CA MUENKE M WILKIE AOM
Citation: Dm. Moloney et al., PREVALENCE OF PRO250ARG MUTATION OF FIBROBLAST GROWTH-FACTOR RECEPTOR-3 IN CORONAL CRANIOSYNOSTOSIS, Lancet, 349(9058), 1997, pp. 1059-1062
MOSAIC TRISOMY-14 WITH HEPATIC INVOLVEMENT
Authors: IGLESIAS A MCCURDY LD GLASS IA COTTER PD ILLUECA M PERENYI A SANSARICQ C
Citation: A. Iglesias et al., MOSAIC TRISOMY-14 WITH HEPATIC INVOLVEMENT, Annales de genetique, 40(2), 1997, pp. 104-108
GENERATION OF SEQUENCE-TAGGED SITES FROM XP22.3 BY ISOLATING COMMON ALU-PCR PRODUCTS OF RADIATION HYBRIDS RETAINING OVERLAPPING HUMAN X-CHROMOSOME FRAGMENTS
Authors: GLASS IA PASSAGE M BERNATOWICZ L SALIDO EC MOHANDAS T YEN PH SHAPIRO LJ
Citation: Ia. Glass et al., GENERATION OF SEQUENCE-TAGGED SITES FROM XP22.3 BY ISOLATING COMMON ALU-PCR PRODUCTS OF RADIATION HYBRIDS RETAINING OVERLAPPING HUMAN X-CHROMOSOME FRAGMENTS, Human genetics, 97(5), 1996, pp. 604-610
GENETIC LOCALIZATION OF MRX27 TO XQ24-26 DEFINES ANOTHER DISCRETE GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION
Authors: GEDEON AK GLASS IA CONNOR JM MULLEY JC
Citation: Ak. Gedeon et al., GENETIC LOCALIZATION OF MRX27 TO XQ24-26 DEFINES ANOTHER DISCRETE GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 64(1), 1996, pp. 121-124
GENETIC-MAPPING OF A CONE AND ROD DYSFUNCTION (ALAND ISLAND EYE DISEASE) TO THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME
Authors: GLASS IA GOOD P COLEMAN MP FULLWOOD P GILES MG LINDSAY S NEMETH AH DAVIES KE WILLSHAW HA FIELDER A KILPATRICK M FARNDON PA
Citation: Ia. Glass et al., GENETIC-MAPPING OF A CONE AND ROD DYSFUNCTION (ALAND ISLAND EYE DISEASE) TO THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME, Journal of Medical Genetics, 30(12), 1993, pp. 1044-1050
Risultati: 1-8 |