Literature DB >> 8912056

Polymorphism analysis of the VNTR locus D17S5 in central Spain.

E Arroyo1, F García-Sánchez, L Prieto, J M Ruiz de la Cuesta, J L Vicario.   

Abstract

The fragment length polymorphism YNZ22 (D17S5) was analysed for a sample of 207 unrelated individuals living in Madrid (Spanish Caucasians) using PCR-methodology and high resolution separation. Hardy-Weinberg expectations (HWE) were calculated after pooling alleles into four groups. No deviations from HWE were detectable using the conventional chi 2-test. The power of discrimination was estimated as 0.96 and the mean paternity exclusion chance as 0.7587. A comparison of the allele frequency distribution with those of other Caucasian groups revealed no major differences.

Mesh:

Year:  1996        PMID: 8912056     DOI: 10.1007/bf01355525

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


  10 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.  Standard calculations for evaluating a blood-group system.

Authors:  R A FISHER
Journal:  Heredity (Edinb)       Date:  1951-04       Impact factor: 3.821

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

Authors:  M Gené; E Huguet; C Sánchez-García; P Moreno; J Corbella; J Mezquita
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

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

Authors:  G T Horn; B Richards; K W Klinger
Journal:  Nucleic Acids Res       Date:  1989-03-11       Impact factor: 16.971

7.  Sampling variances of heterozygosity and genetic distance.

Authors:  M Nei; A K Roychoudhury
Journal:  Genetics       Date:  1974-02       Impact factor: 4.562

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

Authors:  J R Batanian; S A Ledbetter; R K Wolff; Y Nakamura; R White; W B Dobyns; D H Ledbetter
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

9.  Amplification by the polymerase chain reaction of hypervariable regions of the human genome for evaluation of chimerism after bone marrow transplantation.

Authors:  L Ugozzoli; P Yam; L D Petz; G B Ferrara; R E Champlin; S J Forman; D Koyal; R B Wallace
Journal:  Blood       Date:  1991-04-01       Impact factor: 22.113

10.  PCR typing of the locus D17S30 (YNZ22 VNTR) in an Italian population sample.

Authors:  L Buscemi; N Cucurachi; R Mencarelli; B Sisti; A Tagliabracci; S D Ferrara
Journal:  Int J Legal Med       Date:  1994       Impact factor: 2.686

  10 in total

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