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F Marlhens

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Biochemical and Biophysical Research Communications|May 31, 1985
Lowered level of translatable messenger RNAs for manganese superoxide dismutase in human fibroblasts transformed by SV 40F Marlhens, A Nicole, P M Sinet
Nucleic Acids Research|February 11, 1987
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8)F Marlhens, O Delattre, A Bernard, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Nucleic Acids Research|February 11, 1987
RFLP identified by the anonymous DNA segment OL VII A8 at 18q11 (HGM8 no. D18S7)O Delattre, A Bernard, F Marlhens, et al.
Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.
Human Genetics|March 1, 1987
Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormalityJ L Huret, J M Delabar, F Marlhens, et al.
Annales De Genetique|January 1, 1988
Karyotype evolution of the human HBL-100 cell line and mapping of the integration site of SV40 DNAF Marlhens, C Saint-Ruf, P Nardeux, et al.
Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.
Human Genetics|March 1, 1988
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasiaJ Chelly, F Marlhens, B Dutrillaux, et al.
Human Heredity|January 1, 1988
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probeO Delattre, A Bernard, B Malfoy, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Biochemical and Biophysical Research Communications|May 31, 1985
Lowered level of translatable messenger RNAs for manganese superoxide dismutase in human fibroblasts transformed by SV 40F Marlhens, A Nicole, P M Sinet
Nucleic Acids Research|February 11, 1987
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8)F Marlhens, O Delattre, A Bernard, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Nucleic Acids Research|February 11, 1987
RFLP identified by the anonymous DNA segment OL VII A8 at 18q11 (HGM8 no. D18S7)O Delattre, A Bernard, F Marlhens, et al.
Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.
Human Genetics|March 1, 1987
Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormalityJ L Huret, J M Delabar, F Marlhens, et al.
Annales De Genetique|January 1, 1988
Karyotype evolution of the human HBL-100 cell line and mapping of the integration site of SV40 DNAF Marlhens, C Saint-Ruf, P Nardeux, et al.
Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.
Human Genetics|March 1, 1988
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasiaJ Chelly, F Marlhens, B Dutrillaux, et al.
Human Heredity|January 1, 1988
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probeO Delattre, A Bernard, B Malfoy, et al.
Pageof 2