S79320[Secondary Source ID] - Search Results

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A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs.

Maas RL, Jepeal LI, Elfering SL, Holcombe RF, Morton CC, Eddy RL, Byers MG, Shows TB, Leder P. Maas RL, et al. Am J Hum Genet. 1991 Apr;48(4):687-95. Am J Hum Genet. 1991. PMID: 1673046 Free PMC article.

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15.

Phaneuf D, Labelle Y, Bérubé D, Arden K, Cavenee W, Gagné R, Tanguay RM. Phaneuf D, et al. Am J Hum Genet. 1991 Mar;48(3):525-35. Am J Hum Genet. 1991. PMID: 1998338 Free PMC article.

Identification of two independent Japanese mutant HPRT genes using the PCR technique.

Yamada Y, Goto H, Ogasawara N. Yamada Y, et al. Adv Exp Med Biol. 1991;309B:121-4. doi: 10.1007/978-1-4615-7703-4_27. Adv Exp Med Biol. 1991. PMID: 1840476 No abstract available.

The glycine cleavage system: structure of a cDNA encoding human H-protein, and partial characterization of its gene in patients with hyperglycinemias.

Koyata H, Hiraga K. Koyata H, et al. Am J Hum Genet. 1991 Feb;48(2):351-61. Am J Hum Genet. 1991. PMID: 1671321 Free PMC article.

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