PRENATAL EXCLUSION OF HEREDITARY RETINOBLASTOMA
- 1 April 1988
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 331 (8589) , 826
- https://doi.org/10.1016/s0140-6736(88)91687-x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma GeneNew England Journal of Medicine, 1988
- An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United KingdomBritish Journal of Cancer, 1987
- EARLY DIAGNOSIS IN HEREDITARY RETINOBLASTOMA BY DETECTION OF MOLECULAR DELETIONS AT GENE LOCUSThe Lancet, 1987
- A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaNature, 1986
- Prediction of Familial Predisposition to RetinoblastomaNew England Journal of Medicine, 1986
- Deletions of the esterase D locus from a survey of 200 retinoblastoma patientsHuman Genetics, 1986
- A SINGLE-OPERATOR TECHNIQUE FOR FIRST-TRIMESTER CHORION BIOPSYThe Lancet, 1983