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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 karyotypes
M Cammarata, P Di Simone, L Graziano, et al.
American Journal of Medical Genetics
|
September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two cases
G 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 synostosis
R 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 siblings
A 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 siblings
M 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 newborns
M 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 defect
V Insinga, M Pensabene, M Giuffrè, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 60) with videos related to
Sort By:
Page
of 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 karyotypes
M Cammarata, P Di Simone, L Graziano, et al.
American Journal of Medical Genetics
|
September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two cases
G 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 synostosis
R 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 siblings
A 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 siblings
M 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 newborns
M 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 defect
V Insinga, M Pensabene, M Giuffrè, et al.
Page
of 6