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

Date:
1973
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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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    132 ANTENATAL DIAGNOSIS OF GENETIC DISEASE osuccinic aciduria. Neonatal variant with rapid fatal course. Acta paediatrica scandinavica 58, 528-534. Casper, D. J. «& Benjamin, F. (1970). Immunoreactive insulin in amniotic fluid. Obstetrics and Gynecology 35, 389-393. Cassady, G. & Cailliteau, J. (1967). The amniotic fluid in anencephaly. American Journal of Obstetrics and Gynecology 97, 395-399. Cathro, D. M., Bertrand, J. & Coyle, M. G. (1969). Antenatal diagnosis of adren¬ ocortical hyperplasia. Lancet i, 732. Cherry, S. H., Dolger, H., Rosenñeld, R. E. & Kochwa, S. (1969). Amniotic fluid urea nitrogen, uric acid, and creatinine in diabetic pregnancies. Bulletin of the New York Academy of Medicine 45, 46-52. Cherry, S. H., Rosenfield, R. E. «& Kochwa, S. (1970). Mechanism of accumula¬ tion of amniotic fluid pigment in erythroblastosis fetalis. American Journal of Obstetrics and Gynecology 106, 297-302. Cockburn, F., Robins, S. P. & Forfar, J. O. (1970). Free amino acid concentra¬ tions in fetal fluids. British Medical Journal iii, 1 Al-150. Cox, R. P., Douglas, G., Hutzler, J., Lynfield, J. & Dancis, J. (1970). In utero detection of Pompe's disease. Lancet i, 893. Crawfurd, M. d'A. (1971). Personal communication. Dancis, J., Lind, J. & Vara, P. (1960). Transfer of proteins across the human placenta. In The Placenta and Fetal Membranes, pp. 185-190. Edited by C. A. Villee. Baltimore: Williams & Wilkins. Danes, B. S., Queenan, J. T., Gadow, E. C. & Cederqvist, L. L. (1970). Antenatal diagnosis of mucopolysaccharidoses. Lancet i, 946-947. Delecour, M., Monnier, J. C. &, Codaccioni, X. (1970). Connaissances actuelles sur la physiologie et la biochimie du liquide amniotique. Gynécologie et obstétrique (Paris) 69, 511-525. Doran, T. A., Bjerre, S. & Porter, C. J. (1970). Creatinine uric acid, and electro¬ lytes in amniotic fluid. American Journal of Obstetrics and Gynecology 106, 325-331. Edwards, J. H. (1956). Antenatal detection of hereditary disorders. Lancet i, 579. Emery, A. E. H. (1970). Antenatal diagnosis of genetic disease. In Modern Trends in Human Genetics, pp. 267-296. Edited by A. E. H. Emery. Butter- worth: London. Emery, A. E. H., Burt, D., Nelson, M. M. & Scrimgeour, J. B. (1970). Antenatal diagnosis and amino acid composition of amniotic fluid. Lancet i, 1307-1308. Emery, A. E. H. & McKibbin, B. (1971). Catecholamine content of amniotic fluid in c.n.s. malformations. (Unpublished observations.) Emery, A. E. H., Eccleston, D., Scrimgeour, J. B. & Johnstone, M. (1972). Amniotic fluid composition in c.n.s. malformations. Journal of Obstetrics and Gynaecology of the British Commonwealth 19^ 154-158. Emery, A. E. H. (1972). (Unpublished observations.) Emery, A. E. H., Farquhar, J. W. & Timson, J. (1972). Amniotic fluid amino acids in maternal phenylketonuria. Clinica chimica acta 37, 544-546. Fort, A. T. (1971). Prenatal intrusion into the amnion. American Journal of Obstetrics and Gynecology 110, 432-455. Frandsen, V. A. & Stakemann, G. (1964). The site of production of oestrogenic hormones in human pregnancy. Acta endocrinologica {Denmark) 47, 265-276. Friedberg, V. (1955). Untersuchungen über die fetale Urinbildung. Gynaecologia {Basel) 140, 34-^5. Friedland, J., Perle, G., Saifer, A., Schneck, L. & Volk, B. W. (1971). Screening for Tay-Sachs disease in utero using amniotic fluid. Proceedings of the Society for Experimental Biology and Medicine 136, 1297-1298. Frimpter, G. W., Greenberg, A. J., Hilgartner, M. & Fuchs, F. (1967). Cystathio-