Caveats of antenatal diagnosis of Tay-Sachs disease.
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B. Volk | A. Saifer | L. Schneck | C. Valenti | G. Perle | Larry Schneck | Abraham Saifer | Bruno W. Volk | Carlo Valenti
[1] S. Okada. [Tay-Sachs disease]. , 1970, Nihon rinsho. Japanese journal of clinical medicine.
[2] R. G. Price,et al. The demonstration of multiple heat stable forms of N-acetyl- -glucosaminidase in normal human serum. , 1972, Biochimica et biophysica acta.
[3] J. Stirling,et al. Separation and characterisation of N-acetyl- -glucosaminidases A and P from maternal serum. , 1972, Biochimica et biophysica acta.
[4] S. Aronson,et al. Sphingolipids, Sphingolipidoses and Allied Disorders , 1972, Advances in Experimental Medicine and Biology.
[5] J. Leroy,et al. Tay-Sachs Disease: Prenatal Diagnosis , 1971, Science.
[6] K. Suzuki,et al. Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes. , 1971, The Journal of pediatrics.
[7] R. G. Price,et al. Differential assay of human hexosaminidases A and B. , 1970, Biochimica et biophysica acta.
[8] B. Volk,et al. Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresis. , 1970, Clinica chimica acta; international journal of clinical chemistry.
[9] D. Amsterdam,et al. Prenatal diagnosis of Tay-Sachs disease. , 1970, Lancet.
[10] J. O'brien,et al. Tay-Sachs Disease: Generalized Absence of a Beta-D-N-Acetylhexosaminidase Component , 1969, Science.
[11] K. Sandhoff,et al. Variation of β‐N‐acetylhexosaminidase‐pattern in Tay‐Sachs disease , 1969 .
[12] J. Stirling,et al. N-Acetyl-β-glucosaminidases in human spleen , 1968 .