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C. Camaschella

Veröffentlichungen von C. Camaschella zu Camaschella, C. ->
weitere Veröffentlichungen von C. Camaschella:
Allelic association of microsatellites of 6p in Italian hemochromatosis patients (1996)
Allelic association of microsatellites of 6p in Italian hemochromatosis patients (1996)
Dilemmas and progress in mutation detection (1993)
Construction of a genetic map telomeric to HLA-A by microsatellite analysis (1993)
Analysis of microsatellite instability in chronic lymphoproliferative disorders (1996)
Analysis of microsatellite instability in chronic lymphoproliferative disorders (1996)
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine → threonine at position 75 (E 19) of the γ chain (1976)
Electrophoretic separation of ^Aγ and ^Gγ human globin chains in nonidet P-40 (1979)
Simultaneous screening for β-thalassemia mutations by chemical cleavage of mismatch (1991)
A frequent Aγ-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia (1988)
RFLPs of the phenylalanine hydroxylase gene in the Italian population (1989)
Polymorphism of human fetal haemoglobin studied by isoelectric focusing (1980)
G"γ and A"γ globin chains separation and quantitation by isoelectric focusing (1979)
Haplotype distribution and molecular defects of PKU in Italy (1990)
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy (1990)
Veröffentlichungen zu Camaschella, C.
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1
Camaschella, C., Roetto, A., ... Allelic association of microsatellites of 6p in Italian hemochromatosis patients
in: Human genetics , ISSN 1432-1203, Vol. 97 (4. 1996), p. 476-481
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1996
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2
Camaschella, C., Roetto, A., ... Allelic association of microsatellites of 6p in Italian hemochromatosis patients
in: Human genetics , ISSN 1432-1203, Vol. 97 (4. 1996), p. 476-481
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1996
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3
Dianzani, I., Camaschella, C., ... Dilemmas and progress in mutation detection
in: Trends in Genetics, in: Trends in Genetics . - Amsterdam : Elsevier, ISSN 0168-9525, ZDB-ID 2010993-3 Vol. 9, No. 12 (1993), p. 403-405
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1993
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4
Camaschella, C., Roetto, A., ... Construction of a genetic map telomeric to HLA-A by microsatellite analysis
in: Molecular and Cellular Probes, in: Molecular and Cellular Probes . - Amsterdam : Elsevier, ISSN 0890-8508, ZDB-ID 1471391-3 Vol. 7, No. 5 (1993), p. 411-414
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1993
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5
Volpe, G., Gamberi, B., ... Analysis of microsatellite instability in chronic lymphoproliferative disorders
in: Annals of hematology , ISSN 1432-0584, Vol. 72 (2. 1996), p. 67-71
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1996
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6
Volpe, G., Gamberi, B., ... Analysis of microsatellite instability in chronic lymphoproliferative disorders
in: Annals of hematology , ISSN 1432-0584, Vol. 72 (2. 1996), p. 67-71
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1996
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7
Ricco, G., Mazza, U., ... Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine → threonine at position 75 (E 19) of the γ chain
in: Human genetics , ISSN 1432-1203, Vol. 32 (3. 1976), p. 305-313
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1976
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8
Guerrasio, A., Saglio, G., ... Electrophoretic separation of ^Aγ and ^Gγ human globin chains in nonidet P-40
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 99, No. 1 (1979), p. 7-11
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1979
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9
Dianzani, I., Camaschella, C., ... Simultaneous screening for β-thalassemia mutations by chemical cleavage of mismatch
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 11, No. 1 (1991), p. 48-53
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1991
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10
Ottolenghi, S., Camaschella, C., ... A frequent Aγ-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia
in: Human genetics , ISSN 1432-1203, Vol. 79 (1. 1988), p. 13-17
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1988
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11
Dianzani, I., Farinasso, L., ... RFLPs of the phenylalanine hydroxylase gene in the Italian population
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 12 (2. 1989), p. 162-165
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1989
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12
Chen-Marotel, J., Beuzard, Y., ... Polymorphism of human fetal haemoglobin studied by isoelectric focusing
in: FEBS Letters, in: FEBS Letters . - Amsterdam : Elsevier, ISSN 0014-5793, ZDB-ID 1460391-3 Vol. 115, No. 1 (1980), p. 68-70
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1980
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13
Comi, P., Giglioni, B., ... G"γ and A"γ globin chains separation and quantitation by isoelectric focusing
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 87, No. 1 (1979), p. 1-8
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1979
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14
Dianzani, I., Camaschella, C., ... Haplotype distribution and molecular defects of PKU in Italy
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 13 (3. 1990), p. 292-294
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1990
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15
Dianzani, Irma, Devoto, Marcella, ... Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy
in: Human genetics , ISSN 1432-1203, Vol. 86 (1. 1990), p. 69-72
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1990