Antenatal diagnosis of genetic disease / edited by A.E.H. Emery.

Date:
1973
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Antenatal diagnosis of genetic disease / edited by A.E.H. Emery. Source: Wellcome Collection.

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    134 ANTENATAL DIAGNOSIS OF GENETIC DISEASE fluid and maternal blood through pregnancy. Journal of Obstetrics and Gynae¬ cology of the British Commonwealth 78, 505-512. McCurdy, P. R. (1971). Use of genetic linkage for the detection of female carriers of hemophilia. New England Journal of Medicine 285, 218-219. McKay, D. G., Richardson, M. V. & Hertig, A. T. (1958). Studies of the function of early human trophoblast. III. A study of the protein structure of mole fluid, chorionic and amniotic fluids by paper electrophoresis. American Journal of Obstetrics and Gynecology 75, 699-707. McKibbin, В., O'Gorman, L. & Duckworth, T. (1969). Catecholamine metabo¬ lite excretion in spina biñda. Journal of Clinical Pathology 22, 687-689. Mandelbaum, В. & Robinson, A. R. (1966). Amniotic fluid pigment in erythro¬ blastosis fetalis. Obstetrics and Gynecology 28, 118-120. Matalón, R., Dorfman, A., Nadler, H. L. & Jacobson, С. В. (1970). A chemical method for the antenatal diagnosis of mucopolysaccharidoses. Lancet i, 83-84. Merkatz, I. R., New, M. I., Peterson, R. E. & Seaman, M. P. (1969). Prenatal diagnosis of adrenogenital syndrome by amniocentesis. Journal of Pediatrics 75, 977-982. Mitchell, F. L. & Shackleton, C. H. L. (1969). The investigation of steroid metabolism in early infancy. Advances in Clinical Chemistry 12, 141-215. Michie, E. A. (1966). Oestrogen levels in urine and amniotic fluid in pregnancy with live anencephalic foetus and the effect of intra-amniotic injection of sodium dehydroepiandrosterone sulphate on these levels. Acta endocrinologica {Denmark) 51, 535-542. Morrow, G., Schwarz, R. H., Hallock, J. A. & Barness, L. A. (1970). Prenatal detection of methylmalonic acidaemia. Journal of Pediatrics 77, 120-123. Nadler, H. L. & Messina, A. M. (1969). In utero detection of type II glycogenosis (Pompe's disease). Lancet ii, 1277-1278. Nadler, H. L., Bigley, R. H. «& Hug, G. (1970). Prenatal detection of Pompe's disease. Lancet ii, 369-370. Nelson, G. H. (1969). Amniotic fluid phospholipid patterns in normal and ab¬ normal pregnancies. American Journal of Obstetrics and Gynecology 105, 1072-1077. New, M. I. (1970). Antenatal diagnosis of the adrenogenital syndrome. Lancet i, 83. Nichols, J. (1969). Antenatal diagnosis of adrenocortical hyperplasia. Lancet i, 1151-1152. Nichols, J. & Gibson, G. G. (1969). Antenatal diagnosis of the adrenogenital syndrome. Lancet ii, 1068-1069. Nichols, J. (1970). Antenatal diagnosis and treatment of the adrenogenital syndrome. Lancet i, 83. Nichols, J. (1971). Personal communication. O'Brien, J. S., Okada, S., Fillerup, D. L., Veath, M. L., Adomato, В., Brenner, P. H. & Leroy, J. G. (1971). Tay-Sachs disease: prenatal diagnosis. Science, New York 172, 61-64. Ojala, A. (1971). Studies on bilirubin in amniotic fluid with special reference to liver function tests. Dissertation, University of Oulu, Finland. O'Neill, R. T., Morrow, G., Hammel, D., Auerbach, V. H. & Barness, L. A. (1971). Diagnostic significance of amniotic fluid amino acids. Obstetrics and Gynecology 37, 550-554. Ostergard, D. R. (1970). The physiology and clinical importance of amniotic fluid. A review. Obstetrical and Gynecological Survey 25, 297-319. Parmley, T. H. & Miller, E. (1969). Fetal maturity and amniotic fluid analysis.