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Showing results (61-70 of 67) with videos related to

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European Journal of Human Genetics : EJHG|March 14, 2000
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delGP Gasparini, R Rabionet, G Barbujani, et al.
Journal of Medical Genetics|November 25, 2003
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutationsV Annese, A Latiano, O Palmieri, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
The American Journal of Pathology|November 12, 1998
Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathyE Arbustini, M Diegoli, R Fasani, et al.
Journal of Medical Screening|August 13, 1999
Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosisP Gasparini, E Arbustini, G Restagno, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC studyV Annese, A Latiano, P Bovio, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean familiesP Gasparini, X Estivill, V Volpini, et al.
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Showing results (61-70 of 67) with videos related to

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Pageof 7
You have reached the last page of results.This site can display upto 67 results.
European Journal of Human Genetics : EJHG|March 14, 2000
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delGP Gasparini, R Rabionet, G Barbujani, et al.
Journal of Medical Genetics|November 25, 2003
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutationsV Annese, A Latiano, O Palmieri, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
The American Journal of Pathology|November 12, 1998
Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathyE Arbustini, M Diegoli, R Fasani, et al.
Journal of Medical Screening|August 13, 1999
Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosisP Gasparini, E Arbustini, G Restagno, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC studyV Annese, A Latiano, P Bovio, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean familiesP Gasparini, X Estivill, V Volpini, et al.
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