First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency
- 1 December 2000
- journal article
- case report
- Published by Wiley in Prenatal Diagnosis
- Vol. 20 (13) , 1048-1054
- https://doi.org/10.1002/1097-0223(200012)20:13<1048::aid-pd975>3.0.co;2-8
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis*Molecular Human Reproduction, 2000
- Recent advances and future developments in PGDPrenatal Diagnosis, 1999
- O-093. Cytogenetic aspects of early pregnancy failureHuman Reproduction, 1999
- Successful outcome with day 4 embryo transfer after preimplantation diagnosis for genetically transmitted diseasesHuman Reproduction, 1998
- Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletionPrenatal Diagnosis, 1995
- Birth After Preimplantation Diagnosis of the Cystic Fibrosis △F508 Mutation by Polymerase Chain Reaction in Human Embryos Resulting From Intracytoplasmic Sperm Injection With Epididymal SpermPublished by American Medical Association (AMA) ,1994
- Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiencyHuman Genetics, 1989
- Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers.Proceedings of the National Academy of Sciences, 1989
- BIOPSY OF HUMAN PREIMPLANTATION EMBRYOS AND SEXING BY DNA AMPLIFICATIONThe Lancet, 1989
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986