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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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F Marlhens

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Human Genetics|August 1, 1986

The rate of chromosome breakage is age dependent in lymphocytes of adult controlsF Marlhens, W A Achkar, A Aurias, et al.

Nucleic Acids Research|October 26, 1987

Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3O Delattre, A Bernard, B Malfoy, et al.

Nature Genetics|November 5, 1997

Mutations in RPE65 cause Leber's congenital amaurosisF Marlhens, C Bareil, J M Griffoin, et al.

Journal Francais D'Ophtalmologie|January 5, 2001

[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes]C P Hamel, J M Griffoin, C Bazalgette, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Human Genetics|August 1, 1986

The rate of chromosome breakage is age dependent in lymphocytes of adult controlsF Marlhens, W A Achkar, A Aurias, et al.

Nucleic Acids Research|October 26, 1987

Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3O Delattre, A Bernard, B Malfoy, et al.

Nature Genetics|November 5, 1997

Mutations in RPE65 cause Leber's congenital amaurosisF Marlhens, C Bareil, J M Griffoin, et al.

Journal Francais D'Ophtalmologie|January 5, 2001

[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes]C P Hamel, J M Griffoin, C Bazalgette, et al.

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