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G Scarano

Showing results (31-40 of 63) with videos related to

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Clinical Genetics|May 1, 1984
Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesionM Stabile, M L Cavaliere, G Scarano, et al.
American Journal of Medical Genetics|August 1, 1989
CFC syndrome: report on three additional casesG Sorge, F Di Forti, G Scarano, et al.
Birth Defects Original Article Series|January 1, 1996
A case of short-rib syndrome without polydactyly in a stillborn: a new type?G Scarano, M Della Monica, G Capece, et al.
Clinical Genetics|March 1, 1994
Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndromeG Zampino, C Colosimo, F Balducci, et al.
Clinical Genetics|September 1, 2017
Say-Barber-Biesecker-Young-Simpson syndrome and Genitopatellar syndrome: Lumping or splitting?F Lonardo, M S Lonardo, F Acquaviva, et al.
Biochimica Et Biophysica Acta|March 7, 1996
Archaeal elongation factor 1 beta is a dimer. Primary structure, molecular and biochemical propertiesG Raimo, M Masullo, G Savino, et al.
Human Reproduction (Oxford, England)|September 9, 2006
WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case reportA Biason-Lauber, G De Filippo, D Konrad, et al.
Annales De Genetique|January 1, 1982
t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndromeB Dallapiccola, I Bianco, V Brinchi, et al.
Birth Defects Original Article Series|January 1, 1996
Malformation syndromes with kidney dysplasiaM Genuardi, G Scarano, C Tozzi, et al.
Human Mutation|January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfectaM Mottes, M M Gomez Lira, M Valli, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Clinical Genetics|May 1, 1984
Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesionM Stabile, M L Cavaliere, G Scarano, et al.
American Journal of Medical Genetics|August 1, 1989
CFC syndrome: report on three additional casesG Sorge, F Di Forti, G Scarano, et al.
Birth Defects Original Article Series|January 1, 1996
A case of short-rib syndrome without polydactyly in a stillborn: a new type?G Scarano, M Della Monica, G Capece, et al.
Clinical Genetics|March 1, 1994
Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndromeG Zampino, C Colosimo, F Balducci, et al.
Clinical Genetics|September 1, 2017
Say-Barber-Biesecker-Young-Simpson syndrome and Genitopatellar syndrome: Lumping or splitting?F Lonardo, M S Lonardo, F Acquaviva, et al.
Biochimica Et Biophysica Acta|March 7, 1996
Archaeal elongation factor 1 beta is a dimer. Primary structure, molecular and biochemical propertiesG Raimo, M Masullo, G Savino, et al.
Human Reproduction (Oxford, England)|September 9, 2006
WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case reportA Biason-Lauber, G De Filippo, D Konrad, et al.
Annales De Genetique|January 1, 1982
t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndromeB Dallapiccola, I Bianco, V Brinchi, et al.
Birth Defects Original Article Series|January 1, 1996
Malformation syndromes with kidney dysplasiaM Genuardi, G Scarano, C Tozzi, et al.
Human Mutation|January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfectaM Mottes, M M Gomez Lira, M Valli, et al.
Pageof 7