X65232[Secondary Source ID] - Search Results

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Chromosomal localization of four human zinc finger cDNAs.

Huebner K, Druck T, LaForgia S, Lasota J, Croce CM, Lanfrancone L, Donti E, Pengue G, La Mantia G, Pelicci PG, et al. Huebner K, et al. Hum Genet. 1993 Apr;91(3):217-22. doi: 10.1007/BF00218259. Hum Genet. 1993. PMID: 8478004

Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2.

Tzimagiorgis G, Leversha MA, Chroniary K, Goulielmos G, Sargent CA, Ferguson-Smith M, Moschonas NK. Tzimagiorgis G, et al. Hum Genet. 1993 Jun;91(5):433-8. doi: 10.1007/BF00217767. Hum Genet. 1993. PMID: 8314555

The molecular defect in propionic acidemia: exon skipping caused by an 8-bp deletion from an intron in the PCCB allele.

Ohura T, Ogasawara M, Ikeda H, Narisawa K, Tada K. Ohura T, et al. Hum Genet. 1993 Oct;92(4):397-402. doi: 10.1007/BF01247343. Hum Genet. 1993. PMID: 8225321

Identification of a novel T-insertion polymorphism at the DMD locus.

Muntoni F, Cau M, Congiu R, Congia M, Cao A, Melis MA. Muntoni F, et al. Hum Genet. 1993 Aug;92(1):103. doi: 10.1007/BF00216157. Hum Genet. 1993. PMID: 8396066

Two new polymorphisms in introns 2 and 3 of the human porphobilinogen deaminase gene.

Daimon M, Morita Y, Yamatani K, Igarashi M, Fukase N, Ohnuma H, Sugiyama K, Ogawa A, Manaka H, Tominaga M, et al. Daimon M, et al. Hum Genet. 1993 Sep;92(2):115-6. doi: 10.1007/BF00219676. Hum Genet. 1993. PMID: 8103755

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