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G Corsello

Showing results (21-30 of 60) with videos related to

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Minerva Pediatrica|October 15, 1986
[Silver-Russell syndrome. A possible example of genetic heterogenicity]L Giuffrè, V Benigno, M Cammarata, et al.
American Journal of Medical Genetics|June 22, 1999
Rare sex chromosome aneuploidies in humans: report of six patients with 48,XXYY, 49,XXXXY, and 48,XXXX karyotypesM Cammarata, P Di Simone, L Graziano, et al.
American Journal of Medical Genetics|September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two casesG Corsello, M Giuffrè, A Carcione, et al.
Minerva Pediatrica|March 3, 2004
[17 beta hydroxysteroid dehydrogenase deficiency. Clinical, endocrinological and molecular features]S Bertelloni, M C Maggio, S Geraci, et al.
American Journal of Medical Genetics|January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosisR Rizzo, V Pavone, G Corsello, et al.
Minerva Pediatrica|December 31, 1986
[Amniotic fluid stained with meconium as a risk factor in neonatal pathology]L Giuffrè, A Fazzolari, G Corsello, et al.
Klinische Padiatrie|January 1, 1992
Spondylo-costal dysostosis in two siblingsA La Grutta, G Corsello, V Benigno, et al.
Journal of Medical Case Reports|April 25, 2019
Kawasaki disease triggered by parvovirus infection: an atypical case report of two siblingsM C Maggio, R Cimaz, A Alaimo, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Epidemiological study of nonsyndromic hearing loss in Sicilian newbornsM Niceta, C Fabiano, P Sammarco, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 10, 2015
Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defectV Insinga, M Pensabene, M Giuffrè, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
Minerva Pediatrica|October 15, 1986
[Silver-Russell syndrome. A possible example of genetic heterogenicity]L Giuffrè, V Benigno, M Cammarata, et al.
American Journal of Medical Genetics|June 22, 1999
Rare sex chromosome aneuploidies in humans: report of six patients with 48,XXYY, 49,XXXXY, and 48,XXXX karyotypesM Cammarata, P Di Simone, L Graziano, et al.
American Journal of Medical Genetics|September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two casesG Corsello, M Giuffrè, A Carcione, et al.
Minerva Pediatrica|March 3, 2004
[17 beta hydroxysteroid dehydrogenase deficiency. Clinical, endocrinological and molecular features]S Bertelloni, M C Maggio, S Geraci, et al.
American Journal of Medical Genetics|January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosisR Rizzo, V Pavone, G Corsello, et al.
Minerva Pediatrica|December 31, 1986
[Amniotic fluid stained with meconium as a risk factor in neonatal pathology]L Giuffrè, A Fazzolari, G Corsello, et al.
Klinische Padiatrie|January 1, 1992
Spondylo-costal dysostosis in two siblingsA La Grutta, G Corsello, V Benigno, et al.
Journal of Medical Case Reports|April 25, 2019
Kawasaki disease triggered by parvovirus infection: an atypical case report of two siblingsM C Maggio, R Cimaz, A Alaimo, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Epidemiological study of nonsyndromic hearing loss in Sicilian newbornsM Niceta, C Fabiano, P Sammarco, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 10, 2015
Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defectV Insinga, M Pensabene, M Giuffrè, et al.
Pageof 6