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Results: 1-6 |
Results: 6

Authors: TIEU PT BACH G MATYNIA A HWANG M NEUFELD EF
Citation: Pt. Tieu et al., 4 NOVEL MUTATIONS UNDERLYING MILD OR INTERMEDIATE FORMS OF ALPHA-L-IDURONIDASE DEFICIENCY (MPS IS AND MPS IH S)/, Human mutation, 6(1), 1995, pp. 55-59

Authors: TIEU PT MENON K NEUFELD EF
Citation: Pt. Tieu et al., A MUTANT STOP CODON (TAG) IN THE IDUA GENE IS USED AS AN ACCEPTOR SPLICE-SITE IN A PATIENT WITH HURLER-SYNDROME (MPS IH), Human mutation, 3(3), 1994, pp. 333-336

Authors: MOSKOWITZ SM TIEU PT NEUFELD EF
Citation: Sm. Moskowitz et al., MUTATION IN SCHEIE SYNDROME (MPS-IS) - A G-]A TRANSITION CREATES NEW SPLICE SITE IN INTRON 5 OF ONE IDUA ALLELE, Human mutation, 2(2), 1993, pp. 141-144

Authors: MOSKOWITZ SM TIEU PT NEUFELD EF
Citation: Sm. Moskowitz et al., A DELETION INSERTION MUTATION IN THE IDUA GENE IN A LIBYAN JEWISH PATIENT WITH HURLER SYNDROME (MUCOPOLYSACCHARIDOSIS IH), Human mutation, 2(1), 1993, pp. 71-73

Authors: TIEU PT MATYNIA A BACH G HWANG M DLOTT B NEUFELD EF
Citation: Pt. Tieu et al., NOVEL MUTATIONS IN THE GENE ENCODING ALPHA-L-IDURONIDASE IN MUCOPOLYSACCHARIDOSIS-I (MPS I), American journal of human genetics, 53(3), 1993, pp. 955-955

Authors: BACH G MOSKOWITZ SM TIEU PT MATYNIA A NEUFELD EF
Citation: G. Bach et al., MOLECULAR ANALYSIS OF HURLER-SYNDROME IN DRUZE AND MUSLIM ARAB PATIENTS IN ISRAEL - MULTIPLE ALLELIC MUTATIONS OF THE IDUA GENE IN A SMALL GEOGRAPHIC AREA, American journal of human genetics, 53(2), 1993, pp. 330-338
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