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G Pescia

Showing results (91-100 of 117) with videos related to

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Revue Medicale De La Suisse Romande|April 1, 1993
[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]D F Schorderet, F Thonney, N Pillet, et al.
Revue Medicale De La Suisse Romande|September 1, 1979
[Prenatal diagnosis of genetic illnesses. 500 cases]G Pescia, H Nguyen The, D Vajda, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Early screening of fetal aneuploidies (c-beta P/us TEST). Report of 600 observations]G Pescia, P J Ditesheim, C Faway, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies]P Marguerat, D Weihs, G Pescia, et al.
Revue Medicale De La Suisse Romande|February 1, 1985
[Prenatal echographic diagnosis of urinary tract malformations]H Nguyen The, J B Stalder, P De Grandi, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
Andrologia|July 1, 1983
Mosaicism of dynein in spermatozoa and cilia and fibrous sheath aberrations in an infertile manH Walt, A Campana, M Balerna, et al.
Nature Genetics|March 1, 1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesF L Munier, E Korvatska, A Djemaï, et al.
The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.
Prenatal Diagnosis|April 18, 2013
A robust second-generation genome-wide test for fetal aneuploidy based on shotgun sequencing cell-free DNA in maternal bloodN Guex, C Iseli, A Syngelaki, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Revue Medicale De La Suisse Romande|April 1, 1993
[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]D F Schorderet, F Thonney, N Pillet, et al.
Revue Medicale De La Suisse Romande|September 1, 1979
[Prenatal diagnosis of genetic illnesses. 500 cases]G Pescia, H Nguyen The, D Vajda, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Early screening of fetal aneuploidies (c-beta P/us TEST). Report of 600 observations]G Pescia, P J Ditesheim, C Faway, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies]P Marguerat, D Weihs, G Pescia, et al.
Revue Medicale De La Suisse Romande|February 1, 1985
[Prenatal echographic diagnosis of urinary tract malformations]H Nguyen The, J B Stalder, P De Grandi, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
Andrologia|July 1, 1983
Mosaicism of dynein in spermatozoa and cilia and fibrous sheath aberrations in an infertile manH Walt, A Campana, M Balerna, et al.
Nature Genetics|March 1, 1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesF L Munier, E Korvatska, A Djemaï, et al.
The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.
Prenatal Diagnosis|April 18, 2013
A robust second-generation genome-wide test for fetal aneuploidy based on shotgun sequencing cell-free DNA in maternal bloodN Guex, C Iseli, A Syngelaki, et al.
Pageof 12