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M Lerone

Showing results (21-30 of 70) with videos related to

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Haematologica|December 24, 2002
The prevention of the thalassemia maior: emergent problemsL Maffei, E Foglietta, M P Cappabianca, et al.
Human Mutation|January 1, 1997
Startle disease in an Italian family by mutation (K276E): The alpha-subunit of the inhibiting glycine receptorM Seri, A Bolino, L J Galietta, et al.
Human Genetics|October 1, 1991
Multiple sutural synostosis and congenital cataractsM Lerone, G Romeo, E Conrad, 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.
Journal of Medical Genetics|October 1, 1989
Updated results of the thalassaemia prevention programme carried out in LatiumI Bianco, B Graziani, M Lerone, et al.
Human Genetics|August 1, 1994
An MspI polymorphism in the X-specific region proximal to the pseudoautosomal boundary. A new example of a unique "African" marker?F Cruciani, D Sellitto, P Santolamazza, et al.
Journal of Medical Genetics|March 21, 1998
Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?M Silengo, L Silvestro, G Capizzi, et al.
Journal of Medical Genetics|August 1, 1984
A screening programme for the prospective prevention of Mediterranean anaemia in Latium: results of seven years' workI Bianco, B Graziani, M Lerone, et al.
Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 1, 1994
Neuronal intestinal dysplasia: clinical experience in Italian patientsG Martucciello, P E Caffarena, M Lerone, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Haematologica|December 24, 2002
The prevention of the thalassemia maior: emergent problemsL Maffei, E Foglietta, M P Cappabianca, et al.
Human Mutation|January 1, 1997
Startle disease in an Italian family by mutation (K276E): The alpha-subunit of the inhibiting glycine receptorM Seri, A Bolino, L J Galietta, et al.
Human Genetics|October 1, 1991
Multiple sutural synostosis and congenital cataractsM Lerone, G Romeo, E Conrad, 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.
Journal of Medical Genetics|October 1, 1989
Updated results of the thalassaemia prevention programme carried out in LatiumI Bianco, B Graziani, M Lerone, et al.
Human Genetics|August 1, 1994
An MspI polymorphism in the X-specific region proximal to the pseudoautosomal boundary. A new example of a unique "African" marker?F Cruciani, D Sellitto, P Santolamazza, et al.
Journal of Medical Genetics|March 21, 1998
Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?M Silengo, L Silvestro, G Capizzi, et al.
Journal of Medical Genetics|August 1, 1984
A screening programme for the prospective prevention of Mediterranean anaemia in Latium: results of seven years' workI Bianco, B Graziani, M Lerone, et al.
Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 1, 1994
Neuronal intestinal dysplasia: clinical experience in Italian patientsG Martucciello, P E Caffarena, M Lerone, et al.
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