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Minerva Pediatrica
|
October 6, 1972
[Mucopolysaccharidoses. IV. Morphological contribution to the knowledge of mucopolysaccharidosis]
U Magrini, S Scappaticci
Human Genetics
|
January 1, 1982
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome
S Scappaticci, D Cerimele, M Fraccaro
Human Genetics
|
June 1, 1988
Shwachman syndrome and chromosome breakage
M Fraccaro, S Scappaticci, M Aricò
Dermatologica
|
January 1, 1991
Porokeratosis and chromosomal abnormalities
G Orecchia, L Perfetti, S Scappaticci
Cancer Genetics and Cytogenetics
|
October 15, 1989
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma
S Scappaticci, M Fraccaro, G Orecchia
Acta Paediatrica Scandinavica
|
November 1, 1971
Identification of the Y chromosome by the fluorescence technique in an XY-X0 gonadal dysgenesis
F Severi, L Tiepolo, S Scappaticci
Advances in Experimental Medicine and Biology
|
January 1, 1985
A population and cytogenetic study of the Werner syndrome in Sardinia
M Fraccaro, S Scappaticci, D Cerimele
American Journal of Medical Genetics
|
December 1, 1989
Chromosome abnormalities in dyskeratosis congenita
S Scappaticci, M Fraccaro, D Cerimele
Annali Di Ostetricia, Ginecologia, Medicina Perinatale
|
June 1, 1970
[On a case of trisomy 13-15 (47,XY, D+)]
C Zara, S Scappaticci, G Gilardi
Cancer Genetics and Cytogenetics
|
October 1, 1995
Chromosomal abnormalities in tumor and lymphocyte cultures from patients with pituitary adenomas
E Capra, S Scappaticci, M P Spina
Page
of 6
Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Minerva Pediatrica
|
October 6, 1972
[Mucopolysaccharidoses. IV. Morphological contribution to the knowledge of mucopolysaccharidosis]
U Magrini, S Scappaticci
Human Genetics
|
January 1, 1982
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome
S Scappaticci, D Cerimele, M Fraccaro
Human Genetics
|
June 1, 1988
Shwachman syndrome and chromosome breakage
M Fraccaro, S Scappaticci, M Aricò
Dermatologica
|
January 1, 1991
Porokeratosis and chromosomal abnormalities
G Orecchia, L Perfetti, S Scappaticci
Cancer Genetics and Cytogenetics
|
October 15, 1989
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma
S Scappaticci, M Fraccaro, G Orecchia
Acta Paediatrica Scandinavica
|
November 1, 1971
Identification of the Y chromosome by the fluorescence technique in an XY-X0 gonadal dysgenesis
F Severi, L Tiepolo, S Scappaticci
Advances in Experimental Medicine and Biology
|
January 1, 1985
A population and cytogenetic study of the Werner syndrome in Sardinia
M Fraccaro, S Scappaticci, D Cerimele
American Journal of Medical Genetics
|
December 1, 1989
Chromosome abnormalities in dyskeratosis congenita
S Scappaticci, M Fraccaro, D Cerimele
Annali Di Ostetricia, Ginecologia, Medicina Perinatale
|
June 1, 1970
[On a case of trisomy 13-15 (47,XY, D+)]
C Zara, S Scappaticci, G Gilardi
Cancer Genetics and Cytogenetics
|
October 1, 1995
Chromosomal abnormalities in tumor and lymphocyte cultures from patients with pituitary adenomas
E Capra, S Scappaticci, M P Spina
Page
of 6