Detection of the deletion on Yp11.2 in a Chinese population
Author:
Publisher
Elsevier BV
Subject
Genetics,Pathology and Forensic Medicine
Reference43 articles.
1. Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y;Jobling;Hum. Mol. Genet.,2007
2. The human Y chromosome: function, evolution and disease;Quintana-Murci;Forensic Sci. Int.,2001
3. Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations;Yong;Hum. Genet.,2007
4. A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Y(p)11.2 (DYS458-MSY1-AMEL-Y) deletion;Chang;Forensic Sci. Int.,2007
5. A rare mutation in the primer binding region of the amelogenin gene can interfere with gender identification;Shadrach;J. Mol. Diagn.,2004
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1. Analysis of a Yp11.2 region deletion in a Chinese female with Turner syndrome: A case report;Heliyon;2023-04
2. A Comparative Study on the Frequency of Amelogenin Y Deletion in a Brahmin Population of Haryana and Rajasthan State with Other Indian and Global Populations;Russian Journal of Genetics;2022-03
3. A novel mutation at the AMEL primer binding region on the Y chromosome in AMELY negative male;International Journal of Legal Medicine;2022-01-25
4. Forensic Human Y-Chromosome Markers: Principles and Applications;Handbook of DNA Profiling;2022
5. Detection and analysis of null alleles of amelogenin in gender identification;Legal Medicine;2021-09
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