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R Mingarelli

Showing results (21-30 of 84) with videos related to

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Annales De Genetique|January 1, 1991
Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and reviewL Zelante, F Torricelli, S Calvano, et al.
American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.
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.
Skeletal Radiology|July 7, 2005
Quantitative ultrasound of the hand phalanges in a cohort of monozygotic twins: influence of genetic and environmental factorsG Guglielmi, F de Terlizzi, I Torrente, et al.
Prenatal Diagnosis|December 1, 1994
Fetal detection of dup 9p11-12G Calabrese, L Stuppia, P Guanciali-Franchi, et al.
Giornale Italiano Di Cardiologia|February 1, 1994
[Genetics of congenital heart diseases]B Dallapiccola, R Mingarelli, M C Digilio, et al.
Journal of the American College of Cardiology|May 20, 1999
Guidelines for 22q11 deletion screening of patients with conotruncal defectsM C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|July 31, 1995
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndromeM C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotypeA Giannotti, M C Digilio, B Marino, et al.
Pageof 9

Showing results (21-30 of 84) with videos related to

Sort By:
Pageof 9
Annales De Genetique|January 1, 1991
Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and reviewL Zelante, F Torricelli, S Calvano, et al.
American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.
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.
Skeletal Radiology|July 7, 2005
Quantitative ultrasound of the hand phalanges in a cohort of monozygotic twins: influence of genetic and environmental factorsG Guglielmi, F de Terlizzi, I Torrente, et al.
Prenatal Diagnosis|December 1, 1994
Fetal detection of dup 9p11-12G Calabrese, L Stuppia, P Guanciali-Franchi, et al.
Giornale Italiano Di Cardiologia|February 1, 1994
[Genetics of congenital heart diseases]B Dallapiccola, R Mingarelli, M C Digilio, et al.
Journal of the American College of Cardiology|May 20, 1999
Guidelines for 22q11 deletion screening of patients with conotruncal defectsM C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|July 31, 1995
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndromeM C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotypeA Giannotti, M C Digilio, B Marino, et al.
Pageof 9