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Hepatology (Baltimore, Md.)
|
April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian families
C Camaschella, S Fargion, M Sampietro, et al.
Haematologica
|
September 1, 1996
Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes
C Camaschella, S Gonella, R Calabrese, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor gene
A Grifa, A Totaro, J M Rommens, et al.
Biochemical and Biophysical Research Communications
|
October 24, 1998
Cloning of a new gene (FB19) within HLA class I region
A Totaro, A Grifa, M Carella, et al.
Blood
|
April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
A Roetto, A Totaro, A Piperno, et al.
American Journal of Hematology
|
February 1, 1995
Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients
C Camaschella, U Mazza, A Roetto, et al.
Nature Genetics
|
May 10, 2000
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
C Camaschella, A Roetto, A Calì, et al.
Human Molecular Genetics
|
May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F
P Gasparini, L Borgato, A Piperno, et al.
Genomics
|
September 15, 1996
Construction of a YAC contig covering human chromosome 6p22
P Malaspina, A Roetto, F Trettel, et al.
Annals of Hematology
|
February 1, 1996
Analysis of microsatellite instability in chronic lymphoproliferative disorders
G Volpe, B Gamberi, C Pastore, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Hepatology (Baltimore, Md.)
|
April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian families
C Camaschella, S Fargion, M Sampietro, et al.
Haematologica
|
September 1, 1996
Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes
C Camaschella, S Gonella, R Calabrese, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor gene
A Grifa, A Totaro, J M Rommens, et al.
Biochemical and Biophysical Research Communications
|
October 24, 1998
Cloning of a new gene (FB19) within HLA class I region
A Totaro, A Grifa, M Carella, et al.
Blood
|
April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
A Roetto, A Totaro, A Piperno, et al.
American Journal of Hematology
|
February 1, 1995
Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients
C Camaschella, U Mazza, A Roetto, et al.
Nature Genetics
|
May 10, 2000
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
C Camaschella, A Roetto, A Calì, et al.
Human Molecular Genetics
|
May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F
P Gasparini, L Borgato, A Piperno, et al.
Genomics
|
September 15, 1996
Construction of a YAC contig covering human chromosome 6p22
P Malaspina, A Roetto, F Trettel, et al.
Annals of Hematology
|
February 1, 1996
Analysis of microsatellite instability in chronic lymphoproliferative disorders
G Volpe, B Gamberi, C Pastore, et al.
Page
of 4