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M C Silengo

Showing results (1-10 of 28) with videos related to

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Human Genetics|December 15, 1976
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndromeM C Silengo, G Andria
Clinical Genetics|March 1, 1978
Recessive spondylocostal dysostosis: two new casesM C Silengo, S Cavallaro, P Franceschini
Pediatric Radiology|April 19, 1979
Radiological features in trisomy 8M C Silengo, G F Davi, P Franceschini
The Journal of Pediatrics|December 1, 1980
Clinical and genetic aspects of Conradi-Hünermann disease. A report of three familial cases and review of the literatureM C Silengo, L Luzzatti, F N Silverman
Human Genetics|January 1, 1982
Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomaliesM C Silengo, G F Davi, P Franceschini
Pediatric Radiology|October 28, 1977
Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndromeM C Silengo, P Franceschini, A Cerutti, et al.
Clinical Genetics|June 1, 1992
A syndrome of progressive sensorineural deafness and cataract inherited as an autosomal dominant traitA Guala, V Germinetti, F Sebastiani, et al.
Human Genetics|June 27, 1978
Trisomy-8 mosaicism: report of a caseM C Silengo, G Davi, G Crua, et al.
Clinical Genetics|February 1, 1988
Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicismM C Silengo, G Lopez Bell, M Biagioli, et al.
Clinical Genetics|May 1, 1987
Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new casesM C Silengo, G L Bell, M Biagioli, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Human Genetics|December 15, 1976
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndromeM C Silengo, G Andria
Clinical Genetics|March 1, 1978
Recessive spondylocostal dysostosis: two new casesM C Silengo, S Cavallaro, P Franceschini
Pediatric Radiology|April 19, 1979
Radiological features in trisomy 8M C Silengo, G F Davi, P Franceschini
The Journal of Pediatrics|December 1, 1980
Clinical and genetic aspects of Conradi-Hünermann disease. A report of three familial cases and review of the literatureM C Silengo, L Luzzatti, F N Silverman
Human Genetics|January 1, 1982
Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomaliesM C Silengo, G F Davi, P Franceschini
Pediatric Radiology|October 28, 1977
Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndromeM C Silengo, P Franceschini, A Cerutti, et al.
Clinical Genetics|June 1, 1992
A syndrome of progressive sensorineural deafness and cataract inherited as an autosomal dominant traitA Guala, V Germinetti, F Sebastiani, et al.
Human Genetics|June 27, 1978
Trisomy-8 mosaicism: report of a caseM C Silengo, G Davi, G Crua, et al.
Clinical Genetics|February 1, 1988
Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicismM C Silengo, G Lopez Bell, M Biagioli, et al.
Clinical Genetics|May 1, 1987
Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new casesM C Silengo, G L Bell, M Biagioli, et al.
Pageof 3