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Literature DB >> 7599103

Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain).

M Gené¹, E Huguet, C Sánchez-García, P Moreno, J Corbella, J Mezquita.

Abstract

Allele and phenotype frequencies for the YNZ22 locus were determined in a population sample from Catalonia (Spain) using the polymerase chain reaction (PCR). In 311 unrelated individuals, 14 alleles and 56 phenotypes were observed. No deviation from Hardy-Weinberg equilibrium was found. The observed heterozygosity was 81.35%. The YNZ22 polymorphism is useful for paternity testing with a CE value of 70% and an Essen-Möller value of 9.35 (log.).

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Year: 1995 PMID： 7599103 DOI： 10.1007/BF01428412

Source DB: PubMed Journal: Int J Legal Med ISSN： 0937-9827 Impact factor: 2.686

12 in total

1. Population genetics and forensic efficiency data of 4 AMPFLP's.

Authors: S Rand; C Puers; K Skowasch; P Wiegand; B Budowle; B Brinkmann
Journal: Int J Legal Med Date: 1992 Impact factor: 2.686

2. Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations.

Authors: R Deka; S De Croo; L M Yu; R E Ferrell
Journal: Hum Genet Date: 1992 Sep-Oct Impact factor: 4.132

3. Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

Authors: B Budowle; R Chakraborty; A M Giusti; A J Eisenberg; R C Allen
Journal: Am J Hum Genet Date: 1991-01 Impact factor: 11.025

4. PCR amplification of large VNTR alleles of D17S5 (YNZ22) locus.

Authors: J Gécz
Journal: Nucleic Acids Res Date: 1991-10-25 Impact factor: 16.971

5. Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors: Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal: Science Date: 1987-03-27 Impact factor: 47.728

6. Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30].

Authors: Y Nakamura; L Ballard; M Leppert; P O'Connell; G M Lathrop; J M Lalouel; R White
Journal: Nucleic Acids Res Date: 1988-06-24 Impact factor: 16.971

7. Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence.

Authors: R K Wolff; Y Nakamura; R White
Journal: Genomics Date: 1988-11 Impact factor: 5.736

Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain).

1. Population genetics and forensic efficiency data of 4 AMPFLP's.

2. Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations.

3. Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

4. PCR amplification of large VNTR alleles of D17S5 (YNZ22) locus.

5. Variable number of tandem repeat (VNTR) markers for human gene mapping.

6. Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30].

7. Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence.

8. Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction.

9. Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction.

10. Regional DNA hypermethylation at D17S5 precedes 17p structural changes in the progression of renal tumors.

1. Polymorphism analysis of the VNTR locus D17S5 in central Spain.