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J-F Mattei

Showing results (171-180 of 202) with videos related to

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The EMBO Journal|November 1, 1987
Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'C Nguyen, P Pontarotti, D Birnbaum, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Human Genetics|March 1, 1992
Physical mapping of an Xq-proximal interstitial duplication in a maleF Muscatelli, J M Verna, N Philip, et al.
American Journal of Medical Genetics|May 1, 1988
Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile siteC Nguyen, M G Mattei, J A Rey, et al.
American Journal of Medical Genetics|September 1, 1982
AtelosteogenesisP Maroteaux, J Spranger, V Stanescu, et al.
Journal De Genetique Humaine|June 1, 1983
[Encephalopathy related to X fragility: neither inactivation nor deletion of the distal fragment q28 to qter. Enzymatic and morphometric evidence]H Jalbert, M A Baeteman, C Trochet-Royer, et al.
Human Mutation|January 1, 1996
Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin geneC Badens, I Thuret, G Michel, et al.
Presse Medicale (Paris, France : 1983)|April 25, 2001
[Glucose-6-phosphate dehydrogenase et neonatal jaundice]C Badens, M Leclaire, J Collomb, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
Genomics|March 1, 1990
Assignment of the gene for neuroendocrine protein 7B2 (SGNE1 locus) to mouse chromosome region 2[E3-F3] and to human chromosome region 15q11-q15M G Mattei, M Mbikay, B S Sylla, et al.
Pageof 21

Showing results (171-180 of 202) with videos related to

Sort By:
Pageof 21
The EMBO Journal|November 1, 1987
Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'C Nguyen, P Pontarotti, D Birnbaum, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Human Genetics|March 1, 1992
Physical mapping of an Xq-proximal interstitial duplication in a maleF Muscatelli, J M Verna, N Philip, et al.
American Journal of Medical Genetics|May 1, 1988
Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile siteC Nguyen, M G Mattei, J A Rey, et al.
American Journal of Medical Genetics|September 1, 1982
AtelosteogenesisP Maroteaux, J Spranger, V Stanescu, et al.
Journal De Genetique Humaine|June 1, 1983
[Encephalopathy related to X fragility: neither inactivation nor deletion of the distal fragment q28 to qter. Enzymatic and morphometric evidence]H Jalbert, M A Baeteman, C Trochet-Royer, et al.
Human Mutation|January 1, 1996
Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin geneC Badens, I Thuret, G Michel, et al.
Presse Medicale (Paris, France : 1983)|April 25, 2001
[Glucose-6-phosphate dehydrogenase et neonatal jaundice]C Badens, M Leclaire, J Collomb, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
Genomics|March 1, 1990
Assignment of the gene for neuroendocrine protein 7B2 (SGNE1 locus) to mouse chromosome region 2[E3-F3] and to human chromosome region 15q11-q15M G Mattei, M Mbikay, B S Sylla, et al.
Pageof 21