Abstracts - faqs.org

Abstracts

Biological sciences

Search abstracts:
Abstracts » Biological sciences

Rapid clearance of fetal DNA from maternal plasma

Article Abstract:

Clearance of circulating fetal DNA in maternal plasma after delivery has been studied using quantitative PCR analysis of the sex-determining region Y gene as a marker for male fetuses. Plasma samples from 12 women were analyzed 1-42 days after males were born. The mean half-life for circulating fetal DNA was 16.3 min, the range being 4-30 min. Plasma DNA analysis may be less susceptible to false-positive results due to carryover from other pregnancies than detection of fetal cells in maternal blood. The quick clearance may be useful for monitoring feto-maternal events that occur rapidly.

Author: Lau, Tze K., Zhang, Jun, Lo, Y.M. Dennis, Chang, Allan M.Z., Hjelm, N. Magnus, Leung, Tse N.
Publisher: University of Chicago Press
Publication Name: American Journal of Human Genetics
Subject: Biological sciences
ISSN: 0002-9297
Year: 1999
Hong Kong, Research, Usage, Maternal-fetal exchange, Chromosome mapping, Genetic disorders

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis

Article Abstract:

Correlation between genotype and phenotype has been examined in 14 families with autosomal recessive lamellar ichthyosis. The results show no consistent correlation between genetic and clinical classifications, suggesting that existing clinical criteria do not discriminate between the different molecular forms of the disease. Three loci have been associated with lamellar ichthyosis. In families with mutations on the TGM1 gene, seven different missense mutations and one splice mutation have been found.

Author: Hennies, Hans Christian, Reis, Andre, Kuster, Wolfgang, Wiebe, Victor, Krebsova, Alice
Publisher: University of Chicago Press
Publication Name: American Journal of Human Genetics
Subject: Biological sciences
ISSN: 0002-9297
Year: 1998
Genetic aspects, Ichthyosis, Keratinization

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Similar abstracts:
  • Abstracts: Measurement and use of total plasma homocysteine. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis
  • Abstracts: A high rate (10%-30%) of parental consanguinity in cytochrome-oxidase deficiency. Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome
  • Abstracts: A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24
  • Abstracts: Mixed messages: presentation of information in cystic fibrosis-screening pamphlets. Prenatal screening for cystic fibrosis carriers: an economic evaluation
  • Abstracts: Complete genomic structure and mutational spectrum of PHKA2 in patients with X-linked liver glycogenosis Type I and II
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.