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Results: 1-9 |
Results: 9
THE GENE FOR GLYCOGEN-STORAGE-DISEASE TYPE 1B MAPS TO CHROMOSOME 11Q23
Authors: ANNABI B HIRAIWA H MANSFIELD BC LEI KJ UBAGAI T POLYMEROPOULOS MH MOSES SW PARVARI R HERSHKOVITZ E MANDEL H FRYMAN M CHOU JY
Citation: B. Annabi et al., THE GENE FOR GLYCOGEN-STORAGE-DISEASE TYPE 1B MAPS TO CHROMOSOME 11Q23, American journal of human genetics, 62(2), 1998, pp. 400-405
NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA
Authors: CHAMBERLIN ME UBAGAI T MUDD SH PAO VY NGUYEN TK GREENE CL THOMAS JA FREEHAUF C CHOU JY
Citation: Me. Chamberlin et al., NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA, American journal of human genetics, 61(4), 1997, pp. 1448-1448
DOMINANT INHERITANCE OF ISOLATED HYPERMETHIONINEMIA IS ASSOCIATED WITH A MUTATION IN THE HUMAN METHIONINE ADENOSYLTRANSFERASE 1A GENE
Authors: CHAMBERLIN ME UBAGAI T MUDD SH LEVY HL CHOU JY
Citation: Me. Chamberlin et al., DOMINANT INHERITANCE OF ISOLATED HYPERMETHIONINEMIA IS ASSOCIATED WITH A MUTATION IN THE HUMAN METHIONINE ADENOSYLTRANSFERASE 1A GENE, American journal of human genetics, 60(3), 1997, pp. 540-546
DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH DEFECTS IN THE HEPATIC FORM OF METHIONINE ADENOSYL TRANSFERASE
Authors: UBAGAI T CHAMBERLIN ME MUDD SH CHOU JY
Citation: T. Ubagai et al., DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH DEFECTS IN THE HEPATIC FORM OF METHIONINE ADENOSYL TRANSFERASE, The FASEB journal, 10(6), 1996, pp. 2147-2147
DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH METHIONINE ADENOSYLTRANSFERASE I II DEFICIENCY/
Authors: CHAMBERLIN ME UBAGAI T MUDD SH WILSON WG LEONARD JV CHOU JY
Citation: Me. Chamberlin et al., DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH METHIONINE ADENOSYLTRANSFERASE I II DEFICIENCY/, The Journal of clinical investigation, 98(4), 1996, pp. 1021-1027
MOLECULAR-GENETICS OF HEPATIC METHIONINE ADENOSYL-TRANSFERASE DEFICIENCY
Authors: UBAGAI T LEI KJ MUDD HS CHOU JY
Citation: T. Ubagai et al., MOLECULAR-GENETICS OF HEPATIC METHIONINE ADENOSYL-TRANSFERASE DEFICIENCY, The FASEB journal, 9(6), 1995, pp. 1442-1442
MOLECULAR MECHANISMS OF AN INBORN ERROR OF METHIONINE PATHWAY - METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
Authors: UBAGAI T LEI KJ HUANG S MUDD SH LEVY HL CHOU JY
Citation: T. Ubagai et al., MOLECULAR MECHANISMS OF AN INBORN ERROR OF METHIONINE PATHWAY - METHIONINE ADENOSYLTRANSFERASE DEFICIENCY, The Journal of clinical investigation, 96(4), 1995, pp. 1943-1947
PRENATAL-DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY BY POLYMERASE CHAIN-REACTION ANALYSIS
Authors: KATAYAMA S TAKESHITA N YANO T KATAGIRI Y SHIROSITA Y KUBO H HIRAKAWA S UBAGAI T
Citation: S. Katayama et al., PRENATAL-DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY BY POLYMERASE CHAIN-REACTION ANALYSIS, Fetal diagnosis and therapy, 9(6), 1994, pp. 379-384
DELETION DETECTION FOR DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY IN THE JAPANESE POPULATION - COMPARISON BETWEEN THE POLYMERASE CHAIN-REACTION AND THE SOUTHERN BLOT ANALYSIS
Authors: KATAYAMA S TAKESHITA N YANO T UBAGAI T QIU XJ KATAGIRI Y KUBO H HIRAKAWA S
Citation: S. Katayama et al., DELETION DETECTION FOR DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY IN THE JAPANESE POPULATION - COMPARISON BETWEEN THE POLYMERASE CHAIN-REACTION AND THE SOUTHERN BLOT ANALYSIS, JPN J HUM G, 38(2), 1993, pp. 177-184
Risultati: 1-9 |