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Clinical Genetics|September 1, 1995
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IVM C Digilio, A Giannotti, G Pagnotta, et al.
Clinical Dysmorphology|October 1, 1995
Sporadic trichodental dysplasia with microcephaly and mental retardationA Giannotti, M C Digilio, G Albertini, et al.
Human Mutation|February 22, 2002
Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangismM Mangino, E Flex, M C Digilio, et al.
American Journal of Medical Genetics|March 1, 1992
New case of Bartsocas-Papas syndrome surviving at 20 monthsA Giannotti, M C Digilio, L Standoli, et al.
Minerva Pediatrica|January 1, 1992
[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case]A Giannotti, A Alessandri, A Reale, et al.
Pediatric Cardiology|March 15, 2002
Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndromeU Giordano, A Turchetta, A Giannotti, et al.
Images in Paediatric Cardiology|February 28, 2012
Clinical manifestations of Noonan syndromeM Digilio, B Marino
Minerva Pediatrica|June 1, 1991
[The life style and physical activity of the child operated on for congenital cardiopathy]F Drago, M C Digilio, S Giannico, et al.
Cytogenetic and Genome Research|August 17, 2005
Pure trisomy 19p syndrome in an infant with an extra ring chromosomeA Novelli, C Ceccarini, L Bernardini, et al.
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