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Results: 1-25 | 26-28 |
Results: 26-28/28
IDENTIFICATION OF MUTATIONS IN THE ALPHA-L-IDURONIDASE GENE (IDUA) THAT CAUSE HURLER AND SCHEIE SYNDROMES
Authors: SCOTT HS LITJENS T NELSON PV THOMPSON PR BROOKS DA HOPWOOD JJ MORRIS CP
Citation: Hs. Scott et al., IDENTIFICATION OF MUTATIONS IN THE ALPHA-L-IDURONIDASE GENE (IDUA) THAT CAUSE HURLER AND SCHEIE SYNDROMES, American journal of human genetics, 53(5), 1993, pp. 973-986
MUTATION ANALYSIS AND CLINICAL OUTCOME OF PATIENTS WITH HURLER-SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE I-H) UNDERGOING BONE-MARROW TRANSPLANTATION
Authors: WHITLEY CB KRIVIT W RAMSAY NKC KERSEY JH CHANG PN LATCHAW RE BLAZAR BR SCOTT HS NELSON PV MORRIS CP HOPWOOD JJ
Citation: Cb. Whitley et al., MUTATION ANALYSIS AND CLINICAL OUTCOME OF PATIENTS WITH HURLER-SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE I-H) UNDERGOING BONE-MARROW TRANSPLANTATION, American journal of human genetics, 53(3), 1993, pp. 101-101
MUCOPOLYSACCHARIDOSIS TYPE-I (HURLER SYNDROME) - LINKAGE DISEQUILIBRIUM INDICATES THE PRESENCE OF A MAJOR ALLELE
Authors: SCOTT HS NELSON PV COOPER A WRAITH JE HOPWOOD JJ MORRIS CP
Citation: Hs. Scott et al., MUCOPOLYSACCHARIDOSIS TYPE-I (HURLER SYNDROME) - LINKAGE DISEQUILIBRIUM INDICATES THE PRESENCE OF A MAJOR ALLELE, Human genetics, 88(6), 1992, pp. 701-702
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