Rey F - Search Results

1

[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene].

Rey F, Abadie V, Lyonnet S, Berthelon M, Caillaud C, Melle D, Labrune P, Saudubray JM, Munnich A, Rey J. Rey F, et al. Among authors: rey j. Arch Fr Pediatr. 1992 Oct;49(8):705-10. Arch Fr Pediatr. 1992. PMID: 1288453 French.

2

[Intellectual development after relaxing the diet at the age of 5 years in typical phenylketonuria].

Abadie V, Rey F, Plainguet F, Rey J. Abadie V, et al. Among authors: rey j, rey f. Arch Fr Pediatr. 1992 Nov;49(9):773-8. Arch Fr Pediatr. 1992. PMID: 1300964 French.

3

Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal.

Caillaud C, Vilarinho L, Vilarinho A, Rey F, Berthelon M, Santos R, Lyonnet S, Briard ML, Osorio RV, Rey J, et al. Caillaud C, et al. Among authors: rey j, rey f. Hum Genet. 1992 Apr;89(1):69-72. doi: 10.1007/BF00207045. Hum Genet. 1992. PMID: 1349566

4

[What can we expect from identification of mutations of the phenylalanine hydroxylase gene?].

Rey J, Rey F. Rey J, et al. Among authors: rey f. Arch Fr Pediatr. 1992 Jan;49(1):1-3. Arch Fr Pediatr. 1992. PMID: 1550444 Review. French. No abstract available.

5

[Catalog of mutations of the phenylalanine hydroxylase gene].

Rey F, Rey J. Rey F, et al. Among authors: rey j. Arch Fr Pediatr. 1992 Jan;49(1):63-5. Arch Fr Pediatr. 1992. PMID: 1550456 Review. French. No abstract available.

6

Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus.

Berthelon M, Caillaud C, Rey F, Labrune P, Melle D, Feingold J, Frézal J, Briard ML, Farriaux JP, Guibaud P, et al. Berthelon M, et al. Among authors: rey f. Hum Genet. 1991 Feb;86(4):355-8. doi: 10.1007/BF00201832. Hum Genet. 1991. PMID: 1671847

7

Two distinct mutations at a single BamHI site in phenylketonuria.

Melle D, Verelst P, Rey F, Berthelon M, François B, Munnich A, Lyonnet S. Melle D, et al. Among authors: rey f. J Med Genet. 1991 Jan;28(1):38-40. doi: 10.1136/jmg.28.1.38. J Med Genet. 1991. PMID: 1671881 Free PMC article.

8

A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria.

Caillaud C, Lyonnet S, Rey F, Melle D, Frebourg T, Berthelon M, Vilarinho L, Vaz Osorio R, Rey J, Munnich A. Caillaud C, et al. Among authors: rey j, rey f. J Biol Chem. 1991 May 25;266(15):9351-4. J Biol Chem. 1991. PMID: 1709636 Free article.

9

Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria.

Labrune P, Melle D, Rey F, Berthelon M, Caillaud C, Rey J, Munnich A, Lyonnet S. Labrune P, et al. Among authors: rey j, rey f. Am J Hum Genet. 1991 Jun;48(6):1115-20. Am J Hum Genet. 1991. PMID: 2035532 Free PMC article.

10

Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

Lyonnet S, Caillaud C, Rey F, Berthelon M, Frézal J, Rey J, Munnich A. Lyonnet S, et al. Among authors: rey j, rey f. Am J Hum Genet. 1989 Apr;44(4):511-7. Am J Hum Genet. 1989. PMID: 2564729 Free PMC article.

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