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American Journal of Ophthalmology|August 24, 1999
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotypeC Incorvaia, G Lamberti, F Parmeggiani, et al.Human Mutation|July 5, 2001
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTRG Feriotto, A Ferlini, A Ravani, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1986
[Genito-urinary malformations in a regional survey in Emilia Romagna]C Magnani, E Calzolari, G Cocchi, et al.Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Marden-Walker syndrome: case report, nosologic discussion and aspects of counselingL Garavelli, A Donadio, G Banchini, et al.The Science of the Total Environment|October 24, 2001
Risk of birth defects in a population exposed to environmental lead pollutionM Vinceti, S Rovesti, M Bergomi, et al.Annales De Genetique|January 1, 1996
A study on limb reduction defects in six European regionsC Stoll, E Calzolari, M Cornel, et al.Acta Oto-Laryngologica. Supplementum|June 29, 2004
Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated alleleE Gualandi, A Ravani, A Berto, et al.Panminerva Medica|January 1, 1992
Failure in intrauterine contraception. Analysis of 137 cases of unfavourable outcomeE Calzolari, R Masciangelo, G Ciampaglia, et al.Genetic Counseling (Geneva, Switzerland)|February 22, 2008
Paracentric inversion of Yq and review of the literatureV Aiello, N Astolfi, R Gruppioni, et al.Clinical Genetics|January 1, 1993
Characterization of a deleted Y chromosome in a male with Turner stigmataE Calzolari, P Patracchini, P Palazzi, et al.Pageof 9