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R Mingarelli

Showing results (61-70 of 84) with videos related to

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Clinical Genetics|October 1, 1995
Duplication Xp22.2 and pseudoisodicentric Yq detected by FISH and PCR in a sterile maleG Palka, G Calabrese, R Mingarelli, et al.
Annales De Genetique|January 1, 1994
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosisG Calabrese, L Stuppia, R Mingarelli, et al.
Prenatal Diagnosis|June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markersI Torrente, M Mangino, A De Luca, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Journal of Medical Genetics|April 5, 2003
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12E Flex, M Mangino, M Mazzoli, et al.
American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
Journal of Medical Genetics|November 14, 1997
Spondylo-mesomelic-acrodysplasia with joint dislocations and severe combined immunodeficiency: a newly recognised immuno-osseous dysplasiaA Castriota-Scanderbeg, R Mingarelli, G Caramia, et al.
Bone Marrow Transplantation|December 7, 2000
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantationG Calabrese, D Fantasia, P G Franch, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Clinical Genetics|October 1, 1995
Duplication Xp22.2 and pseudoisodicentric Yq detected by FISH and PCR in a sterile maleG Palka, G Calabrese, R Mingarelli, et al.
Annales De Genetique|January 1, 1994
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosisG Calabrese, L Stuppia, R Mingarelli, et al.
Prenatal Diagnosis|June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markersI Torrente, M Mangino, A De Luca, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Journal of Medical Genetics|April 5, 2003
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12E Flex, M Mangino, M Mazzoli, et al.
American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
Journal of Medical Genetics|November 14, 1997
Spondylo-mesomelic-acrodysplasia with joint dislocations and severe combined immunodeficiency: a newly recognised immuno-osseous dysplasiaA Castriota-Scanderbeg, R Mingarelli, G Caramia, et al.
Bone Marrow Transplantation|December 7, 2000
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantationG Calabrese, D Fantasia, P G Franch, et al.
Pageof 9