S Scappaticci|M Fraccaro|G Orecchia - JoVE Visualize

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Cancer Genetics and Cytogenetics|November 1, 1989

Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of MibelliS Scappaticci, S Lambiase, G Orecchia, et al.

Annales De Genetique|January 1, 1990

Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndromeS Scappaticci, A Forabosco, G Borroni, et al.

Human Genetics|January 1, 1982

Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's SyndromeS Scappaticci, D Cerimele, M Fraccaro

Human Genetics|December 23, 1977

Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertileM Fraccaro, P Maraschio, F Pasquali, et al.

Annales De Genetique|September 1, 1977

X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromereP Maraschio, S Scappaticci, E Ferrari, et al.

Cancer Genetics and Cytogenetics|March 1, 1992

Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasiaS Scappaticci, G Arrigoni, E Capra, et al.

Human Genetics|April 1, 1986

Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcomaS Scappaticci, D Cerimele, F Cottoni, et al.

Human Genetics|June 1, 1988

Chromosome abnormalities in tuberous sclerosisS Scappaticci, D Cerimele, M Tondi, et al.

Cancer Genetics and Cytogenetics|October 1, 1992

Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a glucagonoma from two subjects with MEN1S Scappaticci, M L Brandi, E Capra, et al.

Cancer Genetics and Cytogenetics|March 1, 1991

Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1S Scappaticci, P Maraschio, N del Ciotto, et al.

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Showing results (1-10 of 99) with videos related to

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Pageof 10

Cancer Genetics and Cytogenetics|November 1, 1989

Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of MibelliS Scappaticci, S Lambiase, G Orecchia, et al.

Annales De Genetique|January 1, 1990

Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndromeS Scappaticci, A Forabosco, G Borroni, et al.

Human Genetics|January 1, 1982

Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's SyndromeS Scappaticci, D Cerimele, M Fraccaro

Human Genetics|December 23, 1977

Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertileM Fraccaro, P Maraschio, F Pasquali, et al.

Annales De Genetique|September 1, 1977

X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromereP Maraschio, S Scappaticci, E Ferrari, et al.

Cancer Genetics and Cytogenetics|March 1, 1992

Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasiaS Scappaticci, G Arrigoni, E Capra, et al.

Human Genetics|April 1, 1986

Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcomaS Scappaticci, D Cerimele, F Cottoni, et al.

Human Genetics|June 1, 1988

Chromosome abnormalities in tuberous sclerosisS Scappaticci, D Cerimele, M Tondi, et al.

Cancer Genetics and Cytogenetics|October 1, 1992

Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a glucagonoma from two subjects with MEN1S Scappaticci, M L Brandi, E Capra, et al.

Cancer Genetics and Cytogenetics|March 1, 1991

Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1S Scappaticci, P Maraschio, N del Ciotto, et al.

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