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R Mingarelli

Showing results (41-50 of 84) with videos related to

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Clinical Genetics|November 15, 2005
Pachydermoperiostosis: an updateM Castori, L Sinibaldi, R Mingarelli, et al.
American Journal of Medical Genetics|October 1, 1994
Hypoparathyroidism as the major manifestation in two patients with 22q11 deletionsG Scirè, B Dallapiccola, P Iannetti, et al.
Clinical Genetics|November 1, 1994
Patient with de novo 12p+ syndrome identified as dir dup (12) (p13) using subchromosomal painting libraries from somatic cell hybridsL Zelante, S Calvano, B Dallapiccola, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.
Human Genetics|December 1, 1996
Molecular studies in three patients with isodicentric Y chromosomeL Stuppia, G Calabrese, P G Franchi, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Clinical Genetics|April 1, 1997
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter)G Calabrese, A Giannotti, R Mingarelli, et al.
American Journal of Medical Genetics|December 22, 1999
FISH analysis in detecting 9p duplication (p22p24)P Guanciali Franchi, G Calabrese, E Morizio, et al.
American Journal of Human Genetics|December 1, 1996
Widening of a Y-chromosome interval-6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to the RBM1 and DAZ genesL Stuppia, G Calabrese, P G Franchi, et al.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
Clinical Genetics|November 15, 2005
Pachydermoperiostosis: an updateM Castori, L Sinibaldi, R Mingarelli, et al.
American Journal of Medical Genetics|October 1, 1994
Hypoparathyroidism as the major manifestation in two patients with 22q11 deletionsG Scirè, B Dallapiccola, P Iannetti, et al.
Clinical Genetics|November 1, 1994
Patient with de novo 12p+ syndrome identified as dir dup (12) (p13) using subchromosomal painting libraries from somatic cell hybridsL Zelante, S Calvano, B Dallapiccola, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.
Human Genetics|December 1, 1996
Molecular studies in three patients with isodicentric Y chromosomeL Stuppia, G Calabrese, P G Franchi, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Clinical Genetics|April 1, 1997
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter)G Calabrese, A Giannotti, R Mingarelli, et al.
American Journal of Medical Genetics|December 22, 1999
FISH analysis in detecting 9p duplication (p22p24)P Guanciali Franchi, G Calabrese, E Morizio, et al.
American Journal of Human Genetics|December 1, 1996
Widening of a Y-chromosome interval-6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to the RBM1 and DAZ genesL Stuppia, G Calabrese, P G Franchi, et al.
Pageof 9