Fortina P - Search Results

1

Sensitivity, reproducibility, and accuracy in short tandem repeat genotyping using capillary array electrophoresis.

Mansfield ES, Vainer M, Enad S, Barker DL, Harris D, Rappaport E, Fortina P. Mansfield ES, et al. Among authors: fortina p. Genome Res. 1996 Sep;6(9):893-903. doi: 10.1101/gr.6.9.893. Genome Res. 1996. PMID: 8889558 Free article.

2

Rapid sizing of polymorphic microsatellite markers by capillary array electrophoresis.

Mansfield ES, Vainer M, Harris DW, Gasparini P, Estivill X, Surrey S, Fortina P. Mansfield ES, et al. Among authors: fortina p. J Chromatogr A. 1997 Sep 26;781(1-2):295-305. doi: 10.1016/s0021-9673(97)00542-6. J Chromatogr A. 1997. PMID: 9368392 Free article.

3

Analysis of short tandem repeat markers by capillary array electrophoresis.

Mansfield ES, Wilson RB, Fortina P. Mansfield ES, et al. Among authors: fortina p. Methods Mol Biol. 2001;163:151-61. doi: 10.1385/1-59259-116-7:151. Methods Mol Biol. 2001. PMID: 11242940 No abstract available.

4

Nucleic acid detection using non-radioactive labelling methods.

Mansfield ES, Worley JM, McKenzie SE, Surrey S, Rappaport E, Fortina P. Mansfield ES, et al. Among authors: fortina p. Mol Cell Probes. 1995 Jun;9(3):145-56. doi: 10.1006/mcpr.1995.0023. Mol Cell Probes. 1995. PMID: 7477006 Free article. Review.

5

Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies.

Mansfield ES, Robertson JM, Lebo RV, Lucero MY, Mayrand PE, Rappaport E, Parrella T, Sartore M, Surrey S, Fortina P. Mansfield ES, et al. Among authors: fortina p. Am J Med Genet. 1993 Dec 15;48(4):200-8. doi: 10.1002/ajmg.1320480406. Am J Med Genet. 1993. PMID: 7510932

6

Parallel molecular genetic analysis.

McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P. McKenzie SE, et al. Among authors: fortina p. Eur J Hum Genet. 1998 Sep-Oct;6(5):417-29. doi: 10.1038/sj.ejhg.5200218. Eur J Hum Genet. 1998. PMID: 9801865 Review.

7

Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform.

Maris JM, Hii G, Gelfand CA, Varde S, White PS, Rappaport E, Surrey S, Fortina P. Maris JM, et al. Among authors: fortina p. Genome Res. 2005 Aug;15(8):1168-76. doi: 10.1101/gr.3865305. Genome Res. 2005. PMID: 16077016 Free PMC article.

8

Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.

Mansfield ES, Blasband A, Kronick MN, Wrabetz L, Kaplan P, Rappaport E, Sartore M, Parrella T, Surrey S, Fortina P. Mansfield ES, et al. Among authors: fortina p. Mol Cell Probes. 1993 Aug;7(4):311-24. doi: 10.1006/mcpr.1993.1045. Mol Cell Probes. 1993. PMID: 8232348 Free article.

9

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia.

Fortina P, Parrella T, Sartore M, Gottardi E, Gabutti V, Delgrosso K, Mansfield E, Rappaport E, Schwartz E, Camaschella C, et al. Fortina P, et al. Blood. 1994 Jun 1;83(11):3356-62. Blood. 1994. PMID: 8193372 Free article.

10

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N, Milá M, Monica MD, Lutfi J, Shohat M, Mansfield E, Delgrosso K, Rappaport E, Surrey S, Fortina P. Zelante L, et al. Among authors: fortina p. Hum Mol Genet. 1997 Sep;6(9):1605-9. doi: 10.1093/hmg/6.9.1605. Hum Mol Genet. 1997. PMID: 9285800

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