Denaturing high-performance liquid chromatography (DHPLC) is a novel high-capacity technique for detecting new mutations. We have evaluated the sensitivity and specificity of this method in a blind analysis of exon H of the factor IX gene and exon 16 of the neurofibromatosis type 1 gene. Under a single set of conditions for each exon, 55/55 individuals carrying 48 unique mutations were correctly identified as were 55/55 individuals with wildtype alleles. We conclude that DHPLC is a highly sensitive and specific method for mutation detection
Detection of DNA sequence variation is fundamental to the identification of the genomic basis of phe...
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and ...
erozygotes or lack both of these two common HFE mutations, and 15 novel HFE mutations have been desc...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
The identification of mutations in the NF1 gene causing type 1 neurofibromatosis (NF1) has presented...
DHPLC is an efficient method for candidate gene scanning with a high level of automation. Single-bas...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
DR and AJD were FCT research grantees (PIC/IC/82822/2007)Development of a simple mutation directed m...
Abstract Denaturing high performance liquid chromatography is a relatively new method by which heter...
High sensivity and specificity of denaturing high performance liquid chromatography (DHPLC) for muta...
BACKGROUND. Somatic mutations of the epidermal growth factor receptor (EGFR) gene in nonsmall-cell l...
The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abn...
AbstractHemophilia B (HB) is an X-linked recessive disorder characterized by mutations in the clotti...
Neurofibromatosis type 2 (NF2) is an autosomal-dominant disorder caused by mutations in the NF2 gene...
Detection of DNA sequence variation is fundamental to the identification of the genomic basis of phe...
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and ...
erozygotes or lack both of these two common HFE mutations, and 15 novel HFE mutations have been desc...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
The high mutation rate at the NF1 locus results in a wide range of molecular abnormalities. The majo...
The identification of mutations in the NF1 gene causing type 1 neurofibromatosis (NF1) has presented...
DHPLC is an efficient method for candidate gene scanning with a high level of automation. Single-bas...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
DR and AJD were FCT research grantees (PIC/IC/82822/2007)Development of a simple mutation directed m...
Abstract Denaturing high performance liquid chromatography is a relatively new method by which heter...
High sensivity and specificity of denaturing high performance liquid chromatography (DHPLC) for muta...
BACKGROUND. Somatic mutations of the epidermal growth factor receptor (EGFR) gene in nonsmall-cell l...
The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abn...
AbstractHemophilia B (HB) is an X-linked recessive disorder characterized by mutations in the clotti...
Neurofibromatosis type 2 (NF2) is an autosomal-dominant disorder caused by mutations in the NF2 gene...
Detection of DNA sequence variation is fundamental to the identification of the genomic basis of phe...
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and ...
erozygotes or lack both of these two common HFE mutations, and 15 novel HFE mutations have been desc...