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Journal of Medical Genetics
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June 3, 2004
Site directed mutagenesis of hMLH1 exonic splicing enhancers does not correlate with splicing disruption
P Lastella, N Resta, I Miccolis, et al.
Human Mutation
|
January 29, 2003
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients
J Boudeau, A Kieloch, D R Alessi, et al.
Human Molecular Genetics
|
December 23, 1999
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis
G Guanti, N Resta, C Simone, et al.
Forensic Science International. Genetics
|
November 7, 2012
Allele frequencies of the new European Standard Set (ESS) loci in a population of Apulia (Southern Italy)
M Piglionica, S Lonero Baldassarra, E Giardina, et al.
Gut
|
January 13, 2006
Cancer risks in LKB1 germline mutation carriers
H Mehenni, N Resta, J-G Park, et al.
American Journal of Human Genetics
|
November 1, 1993
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)
A Stella, N Resta, M Gentile, et al.
Minerva Anestesiologica
|
March 1, 1976
[Diagnostic and therapeutic difficulties in tetanus]
A Gullo, C Melloni, E Romano, et al.
Clinical Genetics
|
June 6, 2003
Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasia
P Lastella, C Sabbà, G M Lenato, et al.
Journal of Forensic Sciences
|
July 29, 2000
Distribution of HumvWA31, HumFESFPS, HumTH01, HumTPOX, HumCD4, HumCSF1PO alleles in a Southern Italian population sample
N Di Nunno, S L Baldassarra, M Carbonara, et al.
Journal of Medical Genetics
|
January 5, 2002
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family
M Montera, F Piaggio, C Marchese, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 37) with videos related to
Sort By:
Page
of 4
Journal of Medical Genetics
|
June 3, 2004
Site directed mutagenesis of hMLH1 exonic splicing enhancers does not correlate with splicing disruption
P Lastella, N Resta, I Miccolis, et al.
Human Mutation
|
January 29, 2003
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients
J Boudeau, A Kieloch, D R Alessi, et al.
Human Molecular Genetics
|
December 23, 1999
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis
G Guanti, N Resta, C Simone, et al.
Forensic Science International. Genetics
|
November 7, 2012
Allele frequencies of the new European Standard Set (ESS) loci in a population of Apulia (Southern Italy)
M Piglionica, S Lonero Baldassarra, E Giardina, et al.
Gut
|
January 13, 2006
Cancer risks in LKB1 germline mutation carriers
H Mehenni, N Resta, J-G Park, et al.
American Journal of Human Genetics
|
November 1, 1993
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)
A Stella, N Resta, M Gentile, et al.
Minerva Anestesiologica
|
March 1, 1976
[Diagnostic and therapeutic difficulties in tetanus]
A Gullo, C Melloni, E Romano, et al.
Clinical Genetics
|
June 6, 2003
Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasia
P Lastella, C Sabbà, G M Lenato, et al.
Journal of Forensic Sciences
|
July 29, 2000
Distribution of HumvWA31, HumFESFPS, HumTH01, HumTPOX, HumCD4, HumCSF1PO alleles in a Southern Italian population sample
N Di Nunno, S L Baldassarra, M Carbonara, et al.
Journal of Medical Genetics
|
January 5, 2002
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family
M Montera, F Piaggio, C Marchese, et al.
Page
of 4