Fortina P - Search Results

1

Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA.

Kobayashi M, Rappaport E, Blasband A, Semeraro A, Sartore M, Surrey S, Fortina P. Kobayashi M, et al. Among authors: fortina p. Mol Cell Probes. 1995 Jun;9(3):175-82. doi: 10.1006/mcpr.1995.0027. Mol Cell Probes. 1995. PMID: 7477010 Free article.

2

Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Fortina P, Conant R, Parrella T, Rappaport E, Scanlin T, Schwartz E, Robertson JM, Surrey S. Fortina P, et al. Mol Cell Probes. 1992 Aug;6(4):353-6. doi: 10.1016/0890-8508(92)90013-n. Mol Cell Probes. 1992. PMID: 1382222 Free article.

3

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.

4

Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology.

Santacroce R, Ratti A, Caroli F, Foglieni B, Ferraris A, Cremonesi L, Margaglione M, Seri M, Ravazzolo R, Restagno G, Dallapiccola B, Rappaport E, Pollak ES, Surrey S, Ferrari M, Fortina P. Santacroce R, et al. Among authors: fortina p. Clin Chem. 2002 Dec;48(12):2124-30. Clin Chem. 2002. PMID: 12446467

5

Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS).

Fortina P, Dotti G, Conant R, Monokian G, Parrella T, Hitchcock W, Rappaport E, Schwartz E, Surrey S. Fortina P, et al. PCR Methods Appl. 1992 Nov;2(2):163-6. doi: 10.1101/gr.2.2.163. PCR Methods Appl. 1992. PMID: 1477672 Free article.

6

A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent.

Fortina P, Delgrosso K, Werner E, Haines K, Rappaport E, Schwartz E, Surrey S. Fortina P, et al. Hemoglobin. 1991;15(1-2):23-41. doi: 10.3109/03630269109072482. Hemoglobin. 1991. PMID: 1717405

7

Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humans.

Fortina P, Delgrosso K, Rappaport E, Werner E, Ballas S, Schwartz E, Surrey S. Fortina P, et al. Prog Clin Biol Res. 1989;316B:151-9. Prog Clin Biol Res. 1989. PMID: 2575754 No abstract available.

8

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.

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

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.

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