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Journal of Medical Genetics|January 1, 1991
Two distinct mutations at a single BamHI site in phenylketonuriaD Melle, P Verelst, F Rey, et al.American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 24, 2010
Serotonin deficiency in phenylketonuria embryopathyC Roux, M Madani, J M Launay, et al.Journal of Medical Genetics|March 1, 1993
Genetic background of clinical homogeneity of phenylketonuria in PolandJ Jaruzelska, R Matuszak, S Lyonnet, et al.Human Molecular Genetics|January 1, 1993
Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuriaV Abadie, J Jaruzelska, S Lyonnet, et al.American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|May 1, 1997
RET in human development and oncogenesisP Edery, C Eng, A Munnich, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1982
[The incidence of congenital malformations. A five-year study carried out in a Paris maternity unit (author's transl)]C Roux, G Migne, N Mulliez, et al.Pediatrie|January 1, 1992
[Molecular genetics and prenatal diagnosis]S Lyonnet, J M Rozet, C Martin, et al.Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.Pageof 117