A simple and reliable method for the detection of the 30delG mutation of the CX26 gene
- 30 June 2000
- journal article
- Published by Elsevier in Molecular and Cellular Probes
- Vol. 14 (3) , 149-152
- https://doi.org/10.1006/mcpr.2000.0297
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive DeafnessNew England Journal of Medicine, 1998
- Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing LossAmerican Journal of Human Genetics, 1998
- Connexin-26 mutations in sporadic and inherited sensorineural deafnessThe Lancet, 1998
- Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossHuman Mutation, 1998
- Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 GeneHuman Molecular Genetics, 1997
- Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated PopulationsHuman Molecular Genetics, 1997
- Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansHuman Molecular Genetics, 1997
- PCR product quantification by non-radioactive hybridization procedures using an oligonucleotide covalently bound to microwellsMolecular and Cellular Probes, 1993
- Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines.The Journal of cell biology, 1992
- Covalent immobilization of DNA onto polystyrene microwells: The molecules are only bound at the 5′ endAnalytical Biochemistry, 1991