Lichter-Konecki, U; Konecki, D S; DiLella, A G et al. (1988) Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene. Biochemistry 27:2881-5
|
Barnes, B M; Kretzmann, M; Zucker, I et al. (1988) Plasma androgen and gonadotropin levels during hibernation and testicular maturation in golden-mantled ground squirrels. Biol Reprod 38:616-22
|
Woo, S L; DiLella, A G; Marvit, J et al. (1987) Molecular basis of phenylketonuria and recombinant DNA strategies for its therapy. Enzyme 38:207-13
|
DiLella, A G; Woo, S L (1987) Hybridization of genomic DNA to oligonucleotide probes in the presence of tetramethylammonium chloride. Methods Enzymol 152:447-51
|
Chakraborty, R; Lidsky, A S; Daiger, S P et al. (1987) Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet 76:40-6
|
Marvit, J; DiLella, A G; Brayton, K et al. (1987) GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria. Nucleic Acids Res 15:5613-28
|
Guttler, F; Ledley, F D; Lidsky, A S et al. (1987) Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria. J Pediatr 110:68-71
|
Guttler, F; DiLella, A G; Ledley, F D et al. (1987) Molecular biology of phenylketonuria. Eur J Pediatr 146 Suppl 1:A5-11
|
DiLella, A G; Woo, S L (1987) Cloning large segments of genomic DNA using cosmid vectors. Methods Enzymol 152:199-212
|
DiLella, A G; Kwok, S C; Ledley, F D et al. (1986) Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene. Biochemistry 25:743-9
|
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