Caveats of antenatal diagnosis of Tay-Sachs disease.

[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 .