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Humangenetik
|
September 20, 1975
A case of extra small acrocentric bisatellited chromosome in a non mongoloid child
M Furbetta, G Rosi, M Biagioni, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1988
[Determination of HbA2 by a microchromatographic method. Reliability and simplification of the use of prepared columns]
M Furbetta, A Angius, S Rufini, et al.
The New England Journal of Medicine
|
January 24, 1980
Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia
Y W Kan, K Y Lee, M Furbetta, et al.
Annals of the New York Academy of Sciences
|
January 1, 1980
Prenatal diagnosis of beta thalassemia: experience with 133 cases and the effect of fetal blood sampling on child development
A Cao, M Furbetta, A Angius, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction
M A Melis, M Pirastu, R Galanello, et al.
Journal De Genetique Humaine
|
June 1, 1978
[Karyotype 46,XY,22p+ in a male patient (author's transl)]
N Trabalza, M Furbetta, G Rosi, et al.
Hemoglobin
|
January 1, 1984
Hematological phenotype of the double heterozygous state for alpha and beta thalassemia
C Rosatelli, A M Falchi, M T Scalas, et al.
Journal of Medical Genetics
|
October 1, 1979
Prenatal diagnosis of beta-thalassaemia by fetal red cell concentration with anti-AB serum
M Furbetta, C Valenti, A Ximenes, et al.
Journal of Medical Genetics
|
December 1, 1981
Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype
M Furbetta, A Angius, A M Falchi, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Humangenetik
|
September 20, 1975
A case of extra small acrocentric bisatellited chromosome in a non mongoloid child
M Furbetta, G Rosi, M Biagioni, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1988
[Determination of HbA2 by a microchromatographic method. Reliability and simplification of the use of prepared columns]
M Furbetta, A Angius, S Rufini, et al.
The New England Journal of Medicine
|
January 24, 1980
Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia
Y W Kan, K Y Lee, M Furbetta, et al.
Annals of the New York Academy of Sciences
|
January 1, 1980
Prenatal diagnosis of beta thalassemia: experience with 133 cases and the effect of fetal blood sampling on child development
A Cao, M Furbetta, A Angius, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction
M A Melis, M Pirastu, R Galanello, et al.
Journal De Genetique Humaine
|
June 1, 1978
[Karyotype 46,XY,22p+ in a male patient (author's transl)]
N Trabalza, M Furbetta, G Rosi, et al.
Hemoglobin
|
January 1, 1984
Hematological phenotype of the double heterozygous state for alpha and beta thalassemia
C Rosatelli, A M Falchi, M T Scalas, et al.
Journal of Medical Genetics
|
October 1, 1979
Prenatal diagnosis of beta-thalassaemia by fetal red cell concentration with anti-AB serum
M Furbetta, C Valenti, A Ximenes, et al.
Journal of Medical Genetics
|
December 1, 1981
Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype
M Furbetta, A Angius, A M Falchi, et al.
Page
of 4