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Haematologica
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May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?
A Iolascon, V Servedio, R Carbone, et al.
Human Mutation
|
July 12, 2002
Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment
N López-Bigas, S Melchionda, R de Cid, et al.
American Journal of Human Genetics
|
October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity
P Gasparini, M J Calonge, L Bisceglia, et al.
Blood
|
February 1, 1992
BCR breakpoint subregions and blast crisis lineage in CML patients
G Martinelli, A Chiamenti, P Gasparini, et al.
Lancet (London, England)
|
December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern Europe
X Estivill, M Chillon, T Casals, et al.
British Journal of Haematology
|
May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia
C Camaschella, M T Bertero, A Serra, et al.
Genomics
|
October 15, 1996
Genomic structure and organization of the human rBAT gene (SLC3A1)
J Purroy, L Bisceglia, M J Calonge, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies
|
April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative study
P Gasparini, N Cappello, B Dallapiccola, et al.
Human Genetics
|
September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populations
X Estivill, P Gasparini, G Novelli, et al.
Human Genetics
|
April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)
A Totaro, A Grifa, A Roetto, et al.
Page
of 21
Search research articles
Search
Showing results (131-140 of 204) with videos related to
Sort By:
Page
of 21
Haematologica
|
May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?
A Iolascon, V Servedio, R Carbone, et al.
Human Mutation
|
July 12, 2002
Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment
N López-Bigas, S Melchionda, R de Cid, et al.
American Journal of Human Genetics
|
October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity
P Gasparini, M J Calonge, L Bisceglia, et al.
Blood
|
February 1, 1992
BCR breakpoint subregions and blast crisis lineage in CML patients
G Martinelli, A Chiamenti, P Gasparini, et al.
Lancet (London, England)
|
December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern Europe
X Estivill, M Chillon, T Casals, et al.
British Journal of Haematology
|
May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia
C Camaschella, M T Bertero, A Serra, et al.
Genomics
|
October 15, 1996
Genomic structure and organization of the human rBAT gene (SLC3A1)
J Purroy, L Bisceglia, M J Calonge, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies
|
April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative study
P Gasparini, N Cappello, B Dallapiccola, et al.
Human Genetics
|
September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populations
X Estivill, P Gasparini, G Novelli, et al.
Human Genetics
|
April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)
A Totaro, A Grifa, A Roetto, et al.
Page
of 21