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L Cremonesi

Showing results (21-30 of 62) with videos related to

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Clinical Chemistry|March 10, 2001
Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: identification of the new mutation C14GL Cremonesi, A Fumagalli, N Soriani, et al.
Electrophoresis|May 1, 1995
Separation and quantitation of reverse transcriptase polymerase chain reaction fragments of basic fibroblast growth factor by capillary electrophoresis in polymer networksC Gelfi, F Leoncini, P G Righetti, et al.
American Journal of Obstetrics and Gynecology|December 1, 1993
Basic fibroblast growth factor and its receptor messenger ribonucleic acids are expressed in human ovarian epithelial neoplasmsA M Di Blasio, L Cremonesi, P Viganó, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1984
[Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters]M Ferrari, A Cantù Rajnoldi, L Cremonesi, et al.
Clinical Genetics|March 1, 1994
Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian populationC Magnani, L Cremonesi, E Belloni, et al.
Clinical Chemistry and Laboratory Medicine|January 23, 1999
Optimized detection of DNA point mutations by double gradient denaturing gradient gel electrophoresisL Cremonesi, P Carrera, E Cardillo, et al.
Annals of the New York Academy of Sciences|November 16, 2001
Quantitative analysis of fetal DNA in maternal plasma in pathological conditions associated with placental abnormalitiesM Smid, A Vassallo, F Lagona, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation in a sample of 175 Italian cystic fibrosis patientsL Cremonesi, L Ruocco, M Seia, et al.
Human Genetics|September 1, 1995
Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutationsV Brancolini, L Cremonesi, E Belloni, et al.
Human Mutation|January 1, 1992
Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypesL Cremonesi, M Ferrari, E Belloni, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
Clinical Chemistry|March 10, 2001
Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: identification of the new mutation C14GL Cremonesi, A Fumagalli, N Soriani, et al.
Electrophoresis|May 1, 1995
Separation and quantitation of reverse transcriptase polymerase chain reaction fragments of basic fibroblast growth factor by capillary electrophoresis in polymer networksC Gelfi, F Leoncini, P G Righetti, et al.
American Journal of Obstetrics and Gynecology|December 1, 1993
Basic fibroblast growth factor and its receptor messenger ribonucleic acids are expressed in human ovarian epithelial neoplasmsA M Di Blasio, L Cremonesi, P Viganó, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1984
[Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters]M Ferrari, A Cantù Rajnoldi, L Cremonesi, et al.
Clinical Genetics|March 1, 1994
Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian populationC Magnani, L Cremonesi, E Belloni, et al.
Clinical Chemistry and Laboratory Medicine|January 23, 1999
Optimized detection of DNA point mutations by double gradient denaturing gradient gel electrophoresisL Cremonesi, P Carrera, E Cardillo, et al.
Annals of the New York Academy of Sciences|November 16, 2001
Quantitative analysis of fetal DNA in maternal plasma in pathological conditions associated with placental abnormalitiesM Smid, A Vassallo, F Lagona, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation in a sample of 175 Italian cystic fibrosis patientsL Cremonesi, L Ruocco, M Seia, et al.
Human Genetics|September 1, 1995
Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutationsV Brancolini, L Cremonesi, E Belloni, et al.
Human Mutation|January 1, 1992
Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypesL Cremonesi, M Ferrari, E Belloni, et al.
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