J L Serre - JoVE Visualize

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Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1987

Studies on an isolated West Indies population (V): Genetic differentiation, evidence for founder effect and driftJ L Serre, J Séger, S Lanset, et al.

The Journal of Clinical Endocrinology and Metabolism|January 27, 2005

Childhood hypophosphatasia due to a de novo missense mutation in the tissue-nonspecific alkaline phosphatase geneA Taillandier, S-L Sallinen, I Brun-Heath, et al.

Human Molecular Genetics|June 1, 1996

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline rangeE Mornet, C Chateau, M C Hirst, et al.

Human Molecular Genetics|May 20, 1999

Correlations of genotype and phenotype in hypophosphatasiaL Zurutuza, F Muller, J F Gibrat, et al.

Revue Francaise De Transfusion Et Immuno-Hematologie|September 1, 1978

[Genetic analysis of a population with abnormalities of gene frequencies]J C Le Petit, C Le Petit, M Marcelin, et al.

Annales De Genetique|January 1, 1988

[Molecular analysis of the parental origin of trisomy in two families with two children having regular trisomy 21]C Pangalos, J L Serre, M Ghica, et al.

American Journal of Medical Genetics|February 13, 2001

Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothersA Mégarbané, N Waked, E Chouery, et al.

Annales De Genetique|January 1, 1988

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.

Lancet (London, England)|February 20, 1988

Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.

Clinical Genetics|February 1, 1989

Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.

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Showing results (21-30 of 50) with videos related to

Sort By:

Pageof 5

Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1987

Studies on an isolated West Indies population (V): Genetic differentiation, evidence for founder effect and driftJ L Serre, J Séger, S Lanset, et al.

The Journal of Clinical Endocrinology and Metabolism|January 27, 2005

Childhood hypophosphatasia due to a de novo missense mutation in the tissue-nonspecific alkaline phosphatase geneA Taillandier, S-L Sallinen, I Brun-Heath, et al.

Human Molecular Genetics|June 1, 1996

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline rangeE Mornet, C Chateau, M C Hirst, et al.

Human Molecular Genetics|May 20, 1999

Correlations of genotype and phenotype in hypophosphatasiaL Zurutuza, F Muller, J F Gibrat, et al.

Revue Francaise De Transfusion Et Immuno-Hematologie|September 1, 1978

[Genetic analysis of a population with abnormalities of gene frequencies]J C Le Petit, C Le Petit, M Marcelin, et al.

Annales De Genetique|January 1, 1988

[Molecular analysis of the parental origin of trisomy in two families with two children having regular trisomy 21]C Pangalos, J L Serre, M Ghica, et al.

American Journal of Medical Genetics|February 13, 2001

Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothersA Mégarbané, N Waked, E Chouery, et al.

Annales De Genetique|January 1, 1988

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.

Lancet (London, England)|February 20, 1988

Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.

Clinical Genetics|February 1, 1989

Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.

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