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R Mingarelli

Showing results (31-40 of 84) with videos related to

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Clinical Genetics|January 1, 1993
Interstitial deletion del(17) (q21.3q23 or 24.2) syndromeB Dallapiccola, R Mingarelli, C Digilio, et al.
Annales De Genetique|January 1, 1996
Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15qP Iannetti, A Spalice, R Mingarelli, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at riskM P Iampieri, R Mingarelli, E Le Guern, et al.
Prenatal Diagnosis|March 1, 1995
Fetal translocation between chromosomes 2, 18, and 21 resolved by fishI Delaroche, M Sabani, G Calabrese, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|March 31, 2004
[Genetic screenings: state of the art and perspectives for public health]V Romano-Spica, R Mingarelli, S Boccia, et al.
Clinical Genetics|September 1, 1994
Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotypeM C Digilio, R Mingarelli, B Marino, et al.
American Journal of Medical Genetics|March 3, 1998
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cellsG Calabrese, E Morizio, P Guanciali Franchi, et al.
American Journal of Medical Genetics|March 7, 1998
Deletion 8p syndromeM C Digilio, B Marino, P Guccione, et al.
Pediatric Radiology|January 1, 1992
Horseshoe lung: an additional component of the Vater associationM G Obregon, A Giannotti, M C Digilio, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Clinical Genetics|January 1, 1993
Interstitial deletion del(17) (q21.3q23 or 24.2) syndromeB Dallapiccola, R Mingarelli, C Digilio, et al.
Annales De Genetique|January 1, 1996
Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15qP Iannetti, A Spalice, R Mingarelli, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at riskM P Iampieri, R Mingarelli, E Le Guern, et al.
Prenatal Diagnosis|March 1, 1995
Fetal translocation between chromosomes 2, 18, and 21 resolved by fishI Delaroche, M Sabani, G Calabrese, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|March 31, 2004
[Genetic screenings: state of the art and perspectives for public health]V Romano-Spica, R Mingarelli, S Boccia, et al.
Clinical Genetics|September 1, 1994
Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotypeM C Digilio, R Mingarelli, B Marino, et al.
American Journal of Medical Genetics|March 3, 1998
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cellsG Calabrese, E Morizio, P Guanciali Franchi, et al.
American Journal of Medical Genetics|March 7, 1998
Deletion 8p syndromeM C Digilio, B Marino, P Guccione, et al.
Pediatric Radiology|January 1, 1992
Horseshoe lung: an additional component of the Vater associationM G Obregon, A Giannotti, M C Digilio, et al.
Pageof 9