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E Belloni

Showing results (21-30 of 40) with videos related to

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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.
Human Molecular Genetics|August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyS W Scherer, P Poorkaj, H Massa, et al.
Clinical Genetics|June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiencyM J Nowaczyk, M J Huggins, D J Tomkins, et al.
Nuovi Annali D'Igiene E Microbiologia|July 1, 1982
[Epidemiological research on human viral hepatitis in the province of Pavia]C Meloni, E Belloni, A Giorgi, et al.
American Journal of Human Genetics|January 13, 2000
Involvement of the HLXB9 homeobox gene in Currarino syndromeE Belloni, G Martucciello, D Verderio, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
La Radiologia Medica|March 25, 2011
Nonpalpable breast lesions: preoperative radiological guidance in radioguided occult lesion localisation (ROLL)E Belloni, C Canevari, P Panizza, et al.
Ecancermedicalscience|January 26, 2012
Chromosomal rearrangements in acute myeloid leukemia (AML)E Belloni, M Trubia, P Gasparini, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
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.
Human Molecular Genetics|August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyS W Scherer, P Poorkaj, H Massa, et al.
Clinical Genetics|June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiencyM J Nowaczyk, M J Huggins, D J Tomkins, et al.
Nuovi Annali D'Igiene E Microbiologia|July 1, 1982
[Epidemiological research on human viral hepatitis in the province of Pavia]C Meloni, E Belloni, A Giorgi, et al.
American Journal of Human Genetics|January 13, 2000
Involvement of the HLXB9 homeobox gene in Currarino syndromeE Belloni, G Martucciello, D Verderio, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
La Radiologia Medica|March 25, 2011
Nonpalpable breast lesions: preoperative radiological guidance in radioguided occult lesion localisation (ROLL)E Belloni, C Canevari, P Panizza, et al.
Ecancermedicalscience|January 26, 2012
Chromosomal rearrangements in acute myeloid leukemia (AML)E Belloni, M Trubia, P Gasparini, et al.
Pageof 4