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G Pescia

Showing results (111-120 of 117) with videos related to

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Ophthalmic Genetics|March 1, 1997
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastomaF L Munier, F Thonney, A Balmer, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Triple screening for trisomy 21: prospective results of 7039 assessments]G Pescia, M H Dao, D Weihs, et al.
Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1991
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]F Munier, A Balmer, C von Moos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Schweizerische Medizinische Wochenschrift|June 4, 1994
Medical-ethical guidelines for genetic investigations in humansH J Müller, Th Deonna, I Abbt, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
N Erb, P Dürig, U Dietz, et al.
Pageof 12

Showing results (111-120 of 117) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 117 results.
Ophthalmic Genetics|March 1, 1997
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastomaF L Munier, F Thonney, A Balmer, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Triple screening for trisomy 21: prospective results of 7039 assessments]G Pescia, M H Dao, D Weihs, et al.
Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1991
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]F Munier, A Balmer, C von Moos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Schweizerische Medizinische Wochenschrift|June 4, 1994
Medical-ethical guidelines for genetic investigations in humansH J Müller, Th Deonna, I Abbt, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
N Erb, P Dürig, U Dietz, et al.
Pageof 12