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Journal of Pediatric Orthopedics
|
November 1, 1989
Chronic idiopathic hyperphosphatasia and fibrous dysplasia in the same child
U E Pazzaglia, D Barbieri, G Beluffi, et al.
Annals of Surgery
|
April 5, 2000
Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry
L Bertario, A Russo, P Radice, et al.
Cancer Genetics and Cytogenetics
|
February 1, 1994
Granulomatous slack skin: cytogenetic and molecular analyses
P Grammatico, L Balus, S Scarpa, et al.
Cancer Research
|
December 1, 1993
A rapid screening method to detect nonsense and frameshift mutations: identification of disease-causing APC alleles
L Varesco, J Groden, L Spirio, et al.
Annals of Human Genetics
|
October 1, 1994
Age of onset in familial adenomatous polyposis: heterogeneity within families and among APC mutations
S Presciuttini, L Varesco, P Sala, 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.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 2, 2003
Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis
L Bertario, A Russo, P Sala, et al.
Human Mutation
|
February 6, 1998
310 basepair APC deletion with duplication of breakpoint (439ins15del310) in an Italian polyposis patient
V Gismondi, A Bafico, R Biticchi, et al.
Genes, Chromosomes & Cancer
|
July 21, 1998
Chain-terminating mutations in the APC gene lead to alterations in APC RNA and protein concentration
V Gismondi, P Stagnaro, S Pedemonte, et al.
Digestive Diseases and Sciences
|
February 1, 1995
Familial adenomatous polyposis and inflammatory bowel disease associated in two kindreds
C Brignola, C Belloli, G De Simone, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Journal of Pediatric Orthopedics
|
November 1, 1989
Chronic idiopathic hyperphosphatasia and fibrous dysplasia in the same child
U E Pazzaglia, D Barbieri, G Beluffi, et al.
Annals of Surgery
|
April 5, 2000
Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry
L Bertario, A Russo, P Radice, et al.
Cancer Genetics and Cytogenetics
|
February 1, 1994
Granulomatous slack skin: cytogenetic and molecular analyses
P Grammatico, L Balus, S Scarpa, et al.
Cancer Research
|
December 1, 1993
A rapid screening method to detect nonsense and frameshift mutations: identification of disease-causing APC alleles
L Varesco, J Groden, L Spirio, et al.
Annals of Human Genetics
|
October 1, 1994
Age of onset in familial adenomatous polyposis: heterogeneity within families and among APC mutations
S Presciuttini, L Varesco, P Sala, 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.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 2, 2003
Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis
L Bertario, A Russo, P Sala, et al.
Human Mutation
|
February 6, 1998
310 basepair APC deletion with duplication of breakpoint (439ins15del310) in an Italian polyposis patient
V Gismondi, A Bafico, R Biticchi, et al.
Genes, Chromosomes & Cancer
|
July 21, 1998
Chain-terminating mutations in the APC gene lead to alterations in APC RNA and protein concentration
V Gismondi, P Stagnaro, S Pedemonte, et al.
Digestive Diseases and Sciences
|
February 1, 1995
Familial adenomatous polyposis and inflammatory bowel disease associated in two kindreds
C Brignola, C Belloli, G De Simone, et al.
Page
of 5