Amplification failure of the amelogenin gene (AMELX) caused by a primer binding site mutation

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Prenatal Diagnosis

• Publication date

  2009-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/pd.2389PMID 19842109
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Rapid prenatal diagnosis of common chromosome aneuploidies by QF‐PCR, results of 9 years of clinical experience

  2009influential reference
• A rare mutation in the primer binding region of the Amelogenin X homologue gene.

  2009cited by this paper
• Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y.

  2007cited by this paper
• The Amelogenin locus displays a high frequency of X homologue failures in São Tomé Island (West Africa)

  2006influential reference
• A rare mutation in the primer binding region of the amelogenin gene can interfere with gender identification.

  2004influential reference
• Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR).

  2001cited by this paper
• Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

  2000cited by this paper
• Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCR

  1999cited by this paper
• A rapid and quantitative DNA sex test: fluorescence-based PCR analysis of X-Y homologous gene amelogenin.

  1993influential reference
• Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

  1989cited by this paper

• PCR-Based Amplification of Amelogenin Gene for Ovine Sex Determination Using Primers of Different GC Percentage.

  2025cites this paper
• Investigation of Mosaicism Detected in STR Typing

  2021cites this paper
• Molecular Markers for Human Sex Determination in Forensic Genetics Analysis

  2021cites this paper
• Identification and molecular characterisation of an AMEL-X null allele due to an Alu insertion.

  2019cites this paper
• Brother-brother or father-son? How a dropout of AmelX may facilitate the elucidation of a familial relationship

  2019cites this paper
• Forensic parameters and mutation analysis of 23 short tandem repeat (PowerPlex® Fusion System) loci in Fujian Han Chinese population.

  2019cites this paper
• Developmental validation of a 6-dye typing system with 27 loci and application in Han population of China

  2017cites this paper
• Comparing six commercial autosomal STR kits in a large Dutch population sample.

  2014cites this paper
• Detection of the deletion on Yp11.2 in a Chinese population.

  2014cites this paper
• Evaluation of genetic parameters of 22 autosomal STR loci (PowerPlex® Fusion System) in a population sample from Northern Italy

  2014cites this paper
• Evaluation of PowerPlex® Fusion System on samples from forensic casework

  2013cites this paper
• Deletion of amelogenin Y-locus in forensics: literature revision and description of a novel method for sex confirmation.

  2013cites this paper
• Null alleles of the X and Y chromosomal amelogenin gene in a Chinese population

  2012cites this paper
• Toward Optimal Detection of the Common Prenatal Aneuploidies by Quantitative Fluorescent-Polymerase Chain Reaction: Comparison of Two Commercial Assays

  2012cites this paper
• A molecular analysis of three amelogenin negative males in two routine paternity tests.

  2011cites this paper