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M M Rinaldi

Showing results (1-10 of 20) with videos related to

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Nursing Homes|March 1, 1976
Updating job descriptions: a useful toolM M Rinaldi
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1997
Phenotypic variability in the chromosome 9 ringM L Cavaliere, M M Rinaldi, P Castelluccio, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 1995
Spondyloepiphyseal dysplasia tarda and nephrotic syndrome in three siblingsG Lama, N Marrone, M Majorana, et al.
Progress in Lipid Research|November 3, 2025
N-Acylethanolamines in cancer: mechanisms and therapeutic potential of lipid regulators of tumor behaviorM F Nanì, M M Rinaldi, M Miraglia, et al.
Annales De Genetique|January 1, 1983
Clinical features of monosomy 10qterA Zatterale, L Pagano, G Fioretti, et al.
Journal of Medical Genetics|June 1, 1984
Ring (13),t(2;6) associated with familial fragile (16)V Ventruto, A Rinaldi, S Renda, et al.
FEBS Letters|August 10, 2000
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)A Orrico, L Galli, M Falciani, et al.
American Journal of Medical Genetics|December 1, 1983
Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13)V Ventruto, R Pisciotta, S Renda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Pituitary deficiency and lack of gonads in an XY pseudohermaphrodite with beta 39/lepore haemoglobinopathyA Saviano, A Filosa, D Pasquali, et al.
Pathologica|January 1, 1983
[Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases]V Ventruto, B Festa, S Renda, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Nursing Homes|March 1, 1976
Updating job descriptions: a useful toolM M Rinaldi
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1997
Phenotypic variability in the chromosome 9 ringM L Cavaliere, M M Rinaldi, P Castelluccio, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 1995
Spondyloepiphyseal dysplasia tarda and nephrotic syndrome in three siblingsG Lama, N Marrone, M Majorana, et al.
Progress in Lipid Research|November 3, 2025
N-Acylethanolamines in cancer: mechanisms and therapeutic potential of lipid regulators of tumor behaviorM F Nanì, M M Rinaldi, M Miraglia, et al.
Annales De Genetique|January 1, 1983
Clinical features of monosomy 10qterA Zatterale, L Pagano, G Fioretti, et al.
Journal of Medical Genetics|June 1, 1984
Ring (13),t(2;6) associated with familial fragile (16)V Ventruto, A Rinaldi, S Renda, et al.
FEBS Letters|August 10, 2000
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)A Orrico, L Galli, M Falciani, et al.
American Journal of Medical Genetics|December 1, 1983
Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13)V Ventruto, R Pisciotta, S Renda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Pituitary deficiency and lack of gonads in an XY pseudohermaphrodite with beta 39/lepore haemoglobinopathyA Saviano, A Filosa, D Pasquali, et al.
Pathologica|January 1, 1983
[Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases]V Ventruto, B Festa, S Renda, et al.
Pageof 2