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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[The evolution of epilepsy in the most common genetic forms with mental retardation (Down's syndrome and the fragile X syndrome)]R Guerrini, C Dravet, A R Ferrari, et al.The Journal of Biological Chemistry|November 24, 1999
Identification and characterization of a novel siglec, siglec-7, expressed by human natural killer cells and monocytesG Nicoll, J Ni, D Liu, 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.Oncogene|March 1, 1989
Characterization of the HST-related FGF.6 gene, a new member of the fibroblast growth factor gene familyI Marics, J Adelaide, F Raybaud, et al.Mechanisms of Development|June 20, 1998
Tumor necrosis factor receptor associated factor 4 (TRAF4) expression pattern during mouse developmentR Masson, C H Régnier, M P Chenard, et al.Nature|July 16, 1987
A new member of the immunoglobulin superfamily--CTLA-4J F Brunet, F Denizot, M F Luciani, et al.Carcinogenesis|August 30, 2000
Molecular cloning and characterization of the human KIN17 cDNA encoding a component of the UVC response that is conserved among metazoansP Kannouche, P Mauffrey, G Pinon-Lataillade, et al.Molecular Pharmacology|March 1, 1993
Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localizationH Matthes, U Boschert, N Amlaiky, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16A Pallant, A Eskenazi, M G Mattei, et al.Pageof 64