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Results: 1-8 |
Results: 8
CLINICAL LABORATORY METHODS FOR DIAGNOSIS OF THE PORPHYRIAS
Authors: ZAIDER E BICKERS DR
Citation: E. Zaider et Dr. Bickers, CLINICAL LABORATORY METHODS FOR DIAGNOSIS OF THE PORPHYRIAS, Clinics in dermatology, 16(2), 1998, pp. 277-293
MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - A MISSENSE MUTATION IN THE PROTOPORPHYRINOGEN OXIDASE GENE
Authors: FRANK J LAM H ZAIDER E POHFITZPATRICK M CHRISTIANO AM
Citation: J. Frank et al., MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - A MISSENSE MUTATION IN THE PROTOPORPHYRINOGEN OXIDASE GENE, Journal of Medical Genetics, 35(3), 1998, pp. 244-247
VARIEGATE PORPHYRIA - A FRAMESHIFT MUTATION AND A NONSENSE MUTATION IN THE PROTOPORPHYRINOGEN OXIDASE GENE
Authors: FRANK J JUGERT FK ZAIDER E GOERZ G MERK HF POHFITZPATRICK M CHRISTIANO AM
Citation: J. Frank et al., VARIEGATE PORPHYRIA - A FRAMESHIFT MUTATION AND A NONSENSE MUTATION IN THE PROTOPORPHYRINOGEN OXIDASE GENE, Journal of investigative dermatology, 109(3), 1997, pp. 409-409
MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE UNDERLIE VARIEGATE PORPHYRIA
Authors: CSERHALMI PB FRANK J LAM HM ZAIDER E POHFITZPATRICK M CHRISTIANO AM
Citation: Pb. Cserhalmi et al., MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE UNDERLIE VARIEGATE PORPHYRIA, Journal of investigative dermatology, 108(4), 1997, pp. 361-361
CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE
Authors: POHFITZPATRICK M HUANG J ZAIDER E WANG X ROTH P GARCIA O POLLACK S PIOMELLI S
Citation: M. Pohfitzpatrick et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE, Hepatology, 23(1), 1996, pp. 306-306
CONGENITAL ERYTHROPOIETIC PORPHYRIA - CLINICAL, BIOCHEMICAL, AND ENZYMATIC PROFILE OF A SEVERELY AFFECTED INFANT
Authors: HUANG JL ZAIDER E ROTH P GARCIA O POLLACK S POHFITZPATRICK MB
Citation: Jl. Huang et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - CLINICAL, BIOCHEMICAL, AND ENZYMATIC PROFILE OF A SEVERELY AFFECTED INFANT, Journal of the American Academy of Dermatology, 34(5), 1996, pp. 924-927
CONGENITAL ERYTHROPOIETIC PORPHYRIA - PRENATAL-DIAGNOSIS BY PORPHYRINANALYSIS OF AMNIOTIC-FLUID
Authors: POHFITZPATRICK M ZAIDER E PETRELLA R
Citation: M. Pohfitzpatrick et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - PRENATAL-DIAGNOSIS BY PORPHYRINANALYSIS OF AMNIOTIC-FLUID, Journal of investigative dermatology, 106(4), 1996, pp. 272-272
CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE
Authors: POHFITZPATRICK M HUANG J ZAIDER E WANG X ROTH P GARCIA O POLLACK S PIOMELLI S
Citation: M. Pohfitzpatrick et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE, Journal of investigative dermatology, 104(4), 1995, pp. 602-602
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