A Nucaro|A Faedda|A Cao|L Boccone - JoVE Visualize

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Genetic Counseling (Geneva, Switzerland)|February 1, 2003

Partial proximal trisomy 10q syndrome: a new caseA Nucaro, A Faedda, A Cao, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Duplication of the terminal band of the long arm of chromosome 7: a new caseL Boccone, D Gasperini, G Pilloni, et al.

Prenatal Diagnosis|October 1, 1988

Pseudomosaic centric fission of chromosome 4 in amniotic cellsA Nucaro, A M Falchi, G Monni, et al.

American Journal of Medical Genetics|July 1, 1994

Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]L Boccone, A Meloni, A M Falchi, et al.

European Journal of Pediatrics|February 1, 1994

Hypothalamic growth hormone deficiency in a patient with ring chromosome 18A Meloni, L Boccone, L Angius, et al.

Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 1, 1995

Neuroprotection by peptide growth factors against anoxia and nitric oxide toxicity requires modulation of protein kinase CK Maiese, L Boccone

Neuroscience Letters|January 17, 1994

Nitric oxide: a downstream mediator of calcium toxicity in the ischemic cascadeK Maiese, J Wagner, L Boccone

American Journal of Medical Genetics|April 1, 1992

X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-XpterC Cianchetti, F Muntoni, A M Falchi, et al.

Prague Medical Report|December 20, 2012

Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGHV Cabras, A Milia, C Montaldo, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000

Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.

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Showing results (1-10 of 383) with videos related to

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Pageof 39

Genetic Counseling (Geneva, Switzerland)|February 1, 2003

Partial proximal trisomy 10q syndrome: a new caseA Nucaro, A Faedda, A Cao, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Duplication of the terminal band of the long arm of chromosome 7: a new caseL Boccone, D Gasperini, G Pilloni, et al.

Prenatal Diagnosis|October 1, 1988

Pseudomosaic centric fission of chromosome 4 in amniotic cellsA Nucaro, A M Falchi, G Monni, et al.

American Journal of Medical Genetics|July 1, 1994

Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]L Boccone, A Meloni, A M Falchi, et al.

European Journal of Pediatrics|February 1, 1994

Hypothalamic growth hormone deficiency in a patient with ring chromosome 18A Meloni, L Boccone, L Angius, et al.

Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 1, 1995

Neuroprotection by peptide growth factors against anoxia and nitric oxide toxicity requires modulation of protein kinase CK Maiese, L Boccone

Neuroscience Letters|January 17, 1994

Nitric oxide: a downstream mediator of calcium toxicity in the ischemic cascadeK Maiese, J Wagner, L Boccone

American Journal of Medical Genetics|April 1, 1992

X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-XpterC Cianchetti, F Muntoni, A M Falchi, et al.

Prague Medical Report|December 20, 2012

Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGHV Cabras, A Milia, C Montaldo, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000

Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.

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