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A Renieri

Showing results (31-40 of 106) with videos related to

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Molecular Syndromology|December 6, 2011
Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 de novo Deletion in a Patient with Van den Ende-Gupta SyndromeM F Bedeschi, L Colombo, F Mari, et al.
Journal of Medical Genetics|February 24, 2001
Mosaicism in Alport syndrome with genetic counsellingM Bruttini, F Vitelli, I Meloni, et al.
Physical Review Letters|October 3, 2001
Suppression of the sawtooth instability in a storage ring by free-electron laser: an example of nonlinear stabilization by noiseR Bartolini, G Dattoli, L Mezi, et al.
Genomics|March 2, 1999
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)F Vitelli, M Piccini, F Caroli, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|February 27, 2013
Risk assessment scenarios of children's exposure to aflatoxin M1 residues in different milk types from the Greek marketIoannis N Tsakiris, Manolis N Tzatzarakis, Athanasios K Alegakis, et al.
Nephron|January 1, 1993
Alport syndrome with type I membranoproliferative glomerulonephritisM Meroni, A Sessa, G Battini, et al.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.
Clinical Genetics|February 24, 2018
CKAP2L mutation confirms the diagnosis of Filippi syndromeG Capecchi, M Baldassarri, S Ferranti, et al.
International Journal of Molecular Sciences|May 19, 2018
Overview of Cadmium Thyroid Disrupting Effects and MechanismsAleksandra Buha, Vesna Matovic, Biljana Antonijevic, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
Molecular Syndromology|December 6, 2011
Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 de novo Deletion in a Patient with Van den Ende-Gupta SyndromeM F Bedeschi, L Colombo, F Mari, et al.
Journal of Medical Genetics|February 24, 2001
Mosaicism in Alport syndrome with genetic counsellingM Bruttini, F Vitelli, I Meloni, et al.
Physical Review Letters|October 3, 2001
Suppression of the sawtooth instability in a storage ring by free-electron laser: an example of nonlinear stabilization by noiseR Bartolini, G Dattoli, L Mezi, et al.
Genomics|March 2, 1999
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)F Vitelli, M Piccini, F Caroli, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|February 27, 2013
Risk assessment scenarios of children's exposure to aflatoxin M1 residues in different milk types from the Greek marketIoannis N Tsakiris, Manolis N Tzatzarakis, Athanasios K Alegakis, et al.
Nephron|January 1, 1993
Alport syndrome with type I membranoproliferative glomerulonephritisM Meroni, A Sessa, G Battini, et al.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.
Clinical Genetics|February 24, 2018
CKAP2L mutation confirms the diagnosis of Filippi syndromeG Capecchi, M Baldassarri, S Ferranti, et al.
International Journal of Molecular Sciences|May 19, 2018
Overview of Cadmium Thyroid Disrupting Effects and MechanismsAleksandra Buha, Vesna Matovic, Biljana Antonijevic, et al.
Pageof 11