Skip to main content
British Medical Journal logoLink to British Medical Journal
. 1979 Jan 6;1(6155):21–22. doi: 10.1136/bmj.1.6155.21-a

Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.

A H Fensom, P F Benson, C H Rodeck, S Campbell, J D Gould
PMCID: PMC1597518  PMID: 760939

Full text

PDF
21

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Dubowitz V., van Iddekinge B., Rodeck C. H., Campbell S., Singer J. D., Scheuerbrandt G., Moss D. W. Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetus. Lancet. 1978 Jan 14;1(8055):90–90. doi: 10.1016/s0140-6736(78)90021-1. [DOI] [PubMed] [Google Scholar]
  2. Fensom A. H., Benson P. F. Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia. Clin Chim Acta. 1975 Jul 23;62(2):189–194. doi: 10.1016/0009-8981(75)90227-2. [DOI] [PubMed] [Google Scholar]
  3. Fensom A. H., Benson P. F., Blunt S. Prenatal diagnosis of galactosaemia. Br Med J. 1974 Nov 16;4(5941):386–387. doi: 10.1136/bmj.4.5941.386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Rodeck C. H., Campbell S. Early prenatal diagnosis of neural-tube defects by ultrasound-guided fetoscopy. Lancet. 1978 May 27;1(8074):1128–1129. doi: 10.1016/s0140-6736(78)90303-3. [DOI] [PubMed] [Google Scholar]
  5. Rodeck C. H., Campbell S. Sampling pure fetal blood by fetoscopy in second trimester of pregnancy. Br Med J. 1978 Sep 9;2(6139):728–730. doi: 10.1136/bmj.2.6139.728. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES