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A Renieri

Showing results (11-20 of 106) with videos related to

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Human Molecular Genetics|October 1, 1994
A Bg/II polymorphism in the COL4A6 geneA Renieri, L Galli, J Zhou, et al.
Journal of Cellular Physiology|February 4, 2005
Non-syndromic X-linked mental retardation: from a molecular to a clinical point of viewA Renieri, C Pescucci, I Longo, et al.
Human Mutation|January 1, 1996
Unequal homologous crossing over resulting in duplication of 36 base pairs within exon 47 of the COL4A5 gene in a family with Alport syndromeE R Hämäläinen, A Renieri, C Pecoraro, et al.
Brain & Development|October 20, 2006
Seizures and electroencephalographic findings in CDKL5 mutations: case report and reviewS Grosso, A Brogna, S Bazzotti, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
The sex steroids influence on uric acid binding to human plasma proteinsG Morozzi, M S D'Amato, A Fioravanti, et al.
The Journal of Pathology|August 1, 1997
Ultrastructural immunocytochemistry of collagenous and non-collagenous proteins in fast-frozen, freeze-substituted, and low-temperature-embedded renal tissue in Alport syndromeA O Muda, S Rahimi, A Renieri, et al.
International Journal of Clinical & Laboratory Research|January 1, 1992
Molecular characterization of the P and I variants of alpha 1-antitrypsinM Seri, B Magi, C Cellesi, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|November 4, 2005
[Clinical and genetic features of the Alport 'syndromes']C Pescucci, I Longo, F Mari, et al.
American Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3F Vitelli, I Meloni, S Fineschi, et al.
Pageof 11

Showing results (11-20 of 106) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|October 1, 1994
A Bg/II polymorphism in the COL4A6 geneA Renieri, L Galli, J Zhou, et al.
Journal of Cellular Physiology|February 4, 2005
Non-syndromic X-linked mental retardation: from a molecular to a clinical point of viewA Renieri, C Pescucci, I Longo, et al.
Human Mutation|January 1, 1996
Unequal homologous crossing over resulting in duplication of 36 base pairs within exon 47 of the COL4A5 gene in a family with Alport syndromeE R Hämäläinen, A Renieri, C Pecoraro, et al.
Brain & Development|October 20, 2006
Seizures and electroencephalographic findings in CDKL5 mutations: case report and reviewS Grosso, A Brogna, S Bazzotti, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
The sex steroids influence on uric acid binding to human plasma proteinsG Morozzi, M S D'Amato, A Fioravanti, et al.
The Journal of Pathology|August 1, 1997
Ultrastructural immunocytochemistry of collagenous and non-collagenous proteins in fast-frozen, freeze-substituted, and low-temperature-embedded renal tissue in Alport syndromeA O Muda, S Rahimi, A Renieri, et al.
International Journal of Clinical & Laboratory Research|January 1, 1992
Molecular characterization of the P and I variants of alpha 1-antitrypsinM Seri, B Magi, C Cellesi, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|November 4, 2005
[Clinical and genetic features of the Alport 'syndromes']C Pescucci, I Longo, F Mari, et al.
American Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3F Vitelli, I Meloni, S Fineschi, et al.
Pageof 11