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R Mingarelli

Showing results (51-60 of 84) with videos related to

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Annales De Genetique|January 1, 1992
Partial deletion 10p syndrome. Report of two patientsM G Obregon, R Mingarelli, A Giannotti, et al.
Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, 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.
American Journal of Otolaryngology|December 15, 2000
Nasal cartilage aplasia in a family with facioaudiosymphalangism syndromeM G Obregon, M C Digilio, R Mingarelli, et al.
Human Genetics|April 1, 1996
Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridizationG Calabrese, R Mingarelli, P Francalanci, et al.
Human Genetics|October 1, 1995
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndromeA Mari, F Amati, R Mingarelli, et al.
Clinical Genetics|June 18, 2004
High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphismA Novelli, C Ceccarini, L Bernardini, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Annales De Genetique|January 1, 1992
Partial deletion 10p syndrome. Report of two patientsM G Obregon, R Mingarelli, A Giannotti, et al.
Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, 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.
American Journal of Otolaryngology|December 15, 2000
Nasal cartilage aplasia in a family with facioaudiosymphalangism syndromeM G Obregon, M C Digilio, R Mingarelli, et al.
Human Genetics|April 1, 1996
Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridizationG Calabrese, R Mingarelli, P Francalanci, et al.
Human Genetics|October 1, 1995
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndromeA Mari, F Amati, R Mingarelli, et al.
Clinical Genetics|June 18, 2004
High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphismA Novelli, C Ceccarini, L Bernardini, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Pageof 9