Inferior mesenteric vein cannulation for veno-venous bypass during liver transplantation: alternative access in difficult hilar dissection.
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Humans↗
Biomedical subjects
M Ramsay
Publications and source records attributed to M Ramsay.
Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutation.
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Chromosomes, Human, Pair 7↗
A new anonymous marker on chromosome 7, D7S420, identifies a PvuII RFLP.
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Chromosomes, Human, Pair 7↗
A new anonymous marker on chromosome 11, D11S347, detects two TaqI RFLPs.
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Chromosomes, Human, Pair 11↗
A new marker on chromosome 15, D15S74, detects three RFLPs.
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Chromosomes, Human, Pair 15↗
An anonymous single copy probe, D3S153, detects an SstI RFLP.
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Chromosomes, Human, Pair 3↗
An arbitrary single copy DNA sequence VC85 [D1S85] detects a 500 bp insertion/deletion polymorphism on chromosome 1.
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Chromosome Deletion↗
Detection of a 3 allele AvaII RFLP by a single copy anonymous DNA sequence VC75 [D7S404] localized to chromosome 7.
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Alleles↗
An arbitrary single copy sequence VC64 [D1S86] detects a moderate frequency TaqI RFLP on chromosome 1.
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Chromosomes, Human, Pair 1↗
An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4.
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Chromosomes, Human, Pair 4↗
A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.
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Alleles↗
An arbitrary single copy DNA sequence VC85 [D1S85] detects a 500 bp insertion/deletion polymorphism on chromosome 1.
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Chromosome Deletion↗
Detection of a 3 allele AvaII RFLP by a single copy anonymous DNA sequence VC75 [D7S404] localized to chromosome 7.
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Alleles↗
An arbitrary single copy sequence VC64 [D1S86] detects a moderate frequency TaqI RFLP on chromosome 1].
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Chromosomes, Human, Pair 1↗
An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4].
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Chromosomes, Human, Pair 4↗
A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.
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Alleles↗
Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32.
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Chromosome Mapping↗
First trimester prenatal diagnosis by chorionic villus sampling. The Johannesburg experience with 48 cases.
Chorionic villus sampling (CVS) is a first trimester alternative to amniocentesis for the prenatal detection of genetic disorders. Initial experience in 48 patients, in whom transcervical CVS was utilised for the diagnosis of chromosomal, biochemical or molecular disorders, is reported. An adequate villus sample was obtained in all cases and a diagnostic result was achieved in 90% of cases. In this series, the miscarriage rate was 4.2%. It is concluded that CVS appears to be a relatively safe and reliable procedure, but the risk of miscarriage can only be accurately assessed after further investigation.
Chorionic Villi Sampling↗