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P Chiurazzi

Showing results (11-20 of 49) with videos related to

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American Journal of Medical Genetics|July 12, 1996
Significance of linkage disequilibrium between the fragile X locus and its flanking markersP Chiurazzi, J Macpherson, S Sherman, et al.
American Journal of Medical Genetics|July 15, 1994
XLMR genes: update 1994G Neri, P Chiurazzi, J F Arena, et al.
American Journal of Human Genetics|October 1, 1994
Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneityF Gurrieri, M Genuardi, P Chiurazzi, et al.
American Journal of Medical Genetics|April 1, 1992
XLMR genes: update 1992G Neri, P Chiurazzi, F Arena, et al.
American Journal of Medical Genetics|April 20, 1999
XLMR genes: update 1998H Lubs, P Chiurazzi, J Arena, et al.
European Review for Medical and Pharmacological Sciences|August 6, 2019
PipeMAGI: an integrated and validated workflow for analysis of NGS data for clinical diagnosticsG Marceddu, T Dallavilla, G Guerri, et al.
Human Molecular Genetics|February 28, 1998
In vitro reactivation of the FMR1 gene involved in fragile X syndromeP Chiurazzi, M G Pomponi, R Willemsen, et al.
Journal of Medical Genetics|October 1, 1993
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3L Kozák, P Chiurazzi, M Genuardi, et al.
Genomics|March 1, 1997
SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene familyV Lapenta, P Chiurazzi, P van der Spek, et al.
American Journal of Medical Genetics|July 12, 1996
Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan populationP Chiurazzi, G Destro-Bisol, M Genuardi, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 12, 1996
Significance of linkage disequilibrium between the fragile X locus and its flanking markersP Chiurazzi, J Macpherson, S Sherman, et al.
American Journal of Medical Genetics|July 15, 1994
XLMR genes: update 1994G Neri, P Chiurazzi, J F Arena, et al.
American Journal of Human Genetics|October 1, 1994
Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneityF Gurrieri, M Genuardi, P Chiurazzi, et al.
American Journal of Medical Genetics|April 1, 1992
XLMR genes: update 1992G Neri, P Chiurazzi, F Arena, et al.
American Journal of Medical Genetics|April 20, 1999
XLMR genes: update 1998H Lubs, P Chiurazzi, J Arena, et al.
European Review for Medical and Pharmacological Sciences|August 6, 2019
PipeMAGI: an integrated and validated workflow for analysis of NGS data for clinical diagnosticsG Marceddu, T Dallavilla, G Guerri, et al.
Human Molecular Genetics|February 28, 1998
In vitro reactivation of the FMR1 gene involved in fragile X syndromeP Chiurazzi, M G Pomponi, R Willemsen, et al.
Journal of Medical Genetics|October 1, 1993
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3L Kozák, P Chiurazzi, M Genuardi, et al.
Genomics|March 1, 1997
SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene familyV Lapenta, P Chiurazzi, P van der Spek, et al.
American Journal of Medical Genetics|July 12, 1996
Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan populationP Chiurazzi, G Destro-Bisol, M Genuardi, et al.
Pageof 5