1. 1977
  2. The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?

    Neufeld, E. F., Liebaers, I., Epstein, C. J., Yatziv, S., Milunsky, A. & Migeon, B. R., 1977, In : Am J Hum Genet. 29, September, p. 455-461 7 p.

    Research output: Contribution to journalArticle

  3. X-linked Hunter syndrome: the heterozygous phenotype in cell culture

    Migeon, B. R., Sprenkle, J. A., Liebaers, I., Scott, J. F. & Neufeld, E. F., 1977, In : Am J Hum Genet. 29, September, p. 448-454 7 p.

    Research output: Contribution to journalArticle

  4. 1976
  5. Antenatal diagnosis of congenital diseases through cultured amniotic cells: results of 149 amniocenteses.

    Vamos-Hurwitz, E., Petit, P., Liebaers, I., Mathy, M., Rodesch, F., Delhaye, C., Hayez, F. & Mandelbaum, M., 1976, In : Acta Paediatr Belg. 29, April-June, p. 91-98 8 p.

    Research output: Contribution to journalArticle

  6. Genetic counselling for Hunter syndrome

    Epstein, C. J., Yatziv, S., Neufeld, E. F. & Liebaers, I., 1976, In : Lancet. 2, October, p. 737-738 2 p.

    Research output: Contribution to journalArticle

  7. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome

    Liebaers, I. & Neufeld, E. F., 1976, In : Pediatr Res. 10, August, p. 733-736 4 p.

    Research output: Contribution to journalArticle

  8. Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state.

    Neufeld, E. F., Liebaers, I. & Lim, T. W., 1976, In : Adv Exp Med Biol. 68, p. 253-260 8 p.

    Research output: Contribution to journalArticle

  9. 1974
  10. Study of the beta-bexosyminidase separation by electrophoresis in homozygote and heterozygote Tay-Sachs cultured fibroblasts.

    Liebaers, I., Vamos, E. & Mandelbaum, I., 1974, In : Acta Clin Belg. 29, p. 94-97 4 p.

    Research output: Contribution to journalArticle

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