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M C Silengo

Showing results (11-20 of 28) with videos related to

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Clinical Genetics|January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritanceM C Silengo, M Biagioli, G L Bell, et al.
Clinical and Experimental Dermatology|August 12, 2009
A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without cleftingL Sorasio, E Biamino, E Garelli, et al.
Clinical Genetics|August 1, 1990
Heart-hand syndrome II. A report of Tabatznik syndrome with new findingsM C Silengo, M Biagioli, A Guala, et al.
American Journal of Medical Genetics|December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasiaM Lerone, M Soliani, D Corea, et al.
Pediatric Radiology|January 1, 1990
A new syndrome with cerebro-oculo-skeletal-renal involvementM C Silengo, M Lerone, A Pelizza, et al.
Clinical Genetics|February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new caseM Lerone, A Pessagno, A Taccone, et al.
Dermatology (Basel, Switzerland)|February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further caseM Priolo, L Rosaia, M Seri, et al.
Clinical Genetics|March 1, 1981
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardationM C Silengo, L Luzzatti, W R Centerwall, et al.
American Journal of Medical Genetics|January 24, 1998
Ectodermal abnormalities in Kabuki syndromeM Lerone, M Priolo, A Naselli, et al.
Human Genetics|November 16, 1978
Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter)P Franceschini, M C Silengo, G F Davi, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Clinical Genetics|January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritanceM C Silengo, M Biagioli, G L Bell, et al.
Clinical and Experimental Dermatology|August 12, 2009
A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without cleftingL Sorasio, E Biamino, E Garelli, et al.
Clinical Genetics|August 1, 1990
Heart-hand syndrome II. A report of Tabatznik syndrome with new findingsM C Silengo, M Biagioli, A Guala, et al.
American Journal of Medical Genetics|December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasiaM Lerone, M Soliani, D Corea, et al.
Pediatric Radiology|January 1, 1990
A new syndrome with cerebro-oculo-skeletal-renal involvementM C Silengo, M Lerone, A Pelizza, et al.
Clinical Genetics|February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new caseM Lerone, A Pessagno, A Taccone, et al.
Dermatology (Basel, Switzerland)|February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further caseM Priolo, L Rosaia, M Seri, et al.
Clinical Genetics|March 1, 1981
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardationM C Silengo, L Luzzatti, W R Centerwall, et al.
American Journal of Medical Genetics|January 24, 1998
Ectodermal abnormalities in Kabuki syndromeM Lerone, M Priolo, A Naselli, et al.
Human Genetics|November 16, 1978
Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter)P Franceschini, M C Silengo, G F Davi, et al.
Pageof 3