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M Fraccaro

Showing results (11-20 of 64) with videos related to

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American Journal of Medical Genetics|May 1, 1989
A syndrome of primary gonadal failure, short stature, mitral valve prolapse, and mental retardationL Cantalamessa, M Baldini, B Ambrosi, et al.
Human Genetics|September 19, 1978
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effectC Danesino, A D'Azzo, P Maraschio, et al.
Human Genetics|October 1, 1990
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundaryR J Jäger, C Ebensperger, M Fraccaro, et al.
Clinical Genetics|September 1, 1986
The fetal pathology of the XXXXY-syndromeH Rehder, M Fraccaro, C Cuoco, 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|January 19, 1979
A homozygote for a serum albumin variant of the fast typeG Vanzetti, F Porta, L Prencipe, 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 10, 1977
Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18V Vigi, P Maraschio, G Bosi, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, 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.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|May 1, 1989
A syndrome of primary gonadal failure, short stature, mitral valve prolapse, and mental retardationL Cantalamessa, M Baldini, B Ambrosi, et al.
Human Genetics|September 19, 1978
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effectC Danesino, A D'Azzo, P Maraschio, et al.
Human Genetics|October 1, 1990
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundaryR J Jäger, C Ebensperger, M Fraccaro, et al.
Clinical Genetics|September 1, 1986
The fetal pathology of the XXXXY-syndromeH Rehder, M Fraccaro, C Cuoco, 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|January 19, 1979
A homozygote for a serum albumin variant of the fast typeG Vanzetti, F Porta, L Prencipe, 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 10, 1977
Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18V Vigi, P Maraschio, G Bosi, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, 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.
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