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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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F Thonney

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American Journal of Human Genetics|December 5, 1998

Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993

Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.

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.

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.

Human Genetics|August 1, 1997

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotypeM Hergersberg, J Balakrishnan, T Bettecken, et al.

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Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

American Journal of Human Genetics|December 5, 1998

Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993

Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.

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.

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.

Human Genetics|August 1, 1997

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotypeM Hergersberg, J Balakrishnan, T Bettecken, et al.

Pageof 3