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Results: 1-11 |
Results: 11
MUTATION AND POLYMORPHISM ANALYSIS OF THE HUMAN HOMOGENTISATE 1,2-DIOXYGENASE GENE IN ALKAPTONURIA PATIENTS
Authors: DEBERNABE DBV GRANADINO B CHIARELLI I PORFIRIO B MAYATEPEK E AQUARON R MOORE MM FESTEN JJM SANMARTI R PENALVA MA DECORDOBA SR
Citation: Dbv. Debernabe et al., MUTATION AND POLYMORPHISM ANALYSIS OF THE HUMAN HOMOGENTISATE 1,2-DIOXYGENASE GENE IN ALKAPTONURIA PATIENTS, American journal of human genetics, 62(4), 1998, pp. 776-784
EPIDEMIOLOGY AND PROPHYLAXIS OF ENDEMIC GOITER IN THE BWA VILLAGE OF SIRAO (MALI)
Authors: ROUX F BELLIS G RHALY AA MONIER C BISSET JP AQUARON R CHAVENTRE A
Citation: F. Roux et al., EPIDEMIOLOGY AND PROPHYLAXIS OF ENDEMIC GOITER IN THE BWA VILLAGE OF SIRAO (MALI), Collegium antropologicum, 22(1), 1998, pp. 43-49
SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA
Authors: RUFENACHT UB GOUYA L SCHNEIDERYIN X PUY H SCHAFER BW AQUARON R NORDMANN Y MINDER EI DEYBACH JC
Citation: Ub. Rufenacht et al., SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, American journal of human genetics, 62(6), 1998, pp. 1341-1352
TYPE-2 OCULOCUTANEOUS ALBINISM (OCA2) IN ZIMBABWE AND CAMEROON - DISTRIBUTION OF THE 2.7-KB DELETION ALLELE OF THE P GENE
Authors: PURI N DURHAMPIERRE D AQUARON R LUND PM KING RA BRILLIANT MH
Citation: N. Puri et al., TYPE-2 OCULOCUTANEOUS ALBINISM (OCA2) IN ZIMBABWE AND CAMEROON - DISTRIBUTION OF THE 2.7-KB DELETION ALLELE OF THE P GENE, Human genetics, 100(5-6), 1997, pp. 651-656
PORPHYRINS AND PORPHYRIAS - FOREWORD
Authors: AQUARON R
Citation: R. Aquaron, PORPHYRINS AND PORPHYRIAS - FOREWORD, Cellular and molecular biology, 43(1), 1997, pp. 1-1
ACUTE INTERMITTENT PORPHYRIA - RAPID MOLECULAR DIAGNOSIS
Authors: PUY H AQUARON R LAMORIL J ROBREAU AM NORDMANN Y DEYBACH JC
Citation: H. Puy et al., ACUTE INTERMITTENT PORPHYRIA - RAPID MOLECULAR DIAGNOSIS, Cellular and molecular biology, 43(1), 1997, pp. 37-45
HAPLOTYPE AND MUTATIONAL ANALYSIS OF THE HUMAN HOMOGENTISATE 1,2-DIOXYGENASE GENE IN ALKAPTONURIA PATIENTS
Authors: DECORDOBA SR DEBERNABE DBV GRANADINO B ESTEBANEZ MC PORFIRIO B MAYATEPEK E AQUARON R PEALVA MA
Citation: Sr. Decordoba et al., HAPLOTYPE AND MUTATIONAL ANALYSIS OF THE HUMAN HOMOGENTISATE 1,2-DIOXYGENASE GENE IN ALKAPTONURIA PATIENTS, American journal of human genetics, 61(4), 1997, pp. 1514-1514
ACUTE INTERMITTENT PORPHYRIA IN 2 MOROCCA N FAMILIES - CLINICAL AND BIOLOGICAL STUDIES
Authors: AQUARON R ZARROUCK K ELBOUSSAKI A ACQUAVIVA JE
Citation: R. Aquaron et al., ACUTE INTERMITTENT PORPHYRIA IN 2 MOROCCA N FAMILIES - CLINICAL AND BIOLOGICAL STUDIES, La Revue de medecine interne, 17(6), 1996, pp. 477-481
PARKINSONISM WITH ALKAPTONURIA - COINCIDENTALLY ASSOCIATION OR STRIATONIGRAL OCHRONOSIS
Authors: AQUARON R FAYET G BARTHET C DESIRE S VIALLET F
Citation: R. Aquaron et al., PARKINSONISM WITH ALKAPTONURIA - COINCIDENTALLY ASSOCIATION OR STRIATONIGRAL OCHRONOSIS, Revue neurologique, 151(1), 1995, pp. 63-66
AFRICAN ORIGIN OF AN INTRAGENIC DELETION OF THE HUMAN-P GENE IN TYROSINASE POSITIVE OCULOCUTANEOUS ALBINISM
Authors: DURHAMPIERRE D GARDNER JM NAKATSU Y KING RA FRANCKE U CHING A AQUARON R DELMARMOL V BRILLIANT MH
Citation: D. Durhampierre et al., AFRICAN ORIGIN OF AN INTRAGENIC DELETION OF THE HUMAN-P GENE IN TYROSINASE POSITIVE OCULOCUTANEOUS ALBINISM, Nature genetics, 7(2), 1994, pp. 176-179
HUMAN OCULOCUTANEOUS ALBINISM - FROM CLIN ICAL OBSERVATION TO MOLECULAR-BIOLOGY
Authors: AQUARON R
Citation: R. Aquaron, HUMAN OCULOCUTANEOUS ALBINISM - FROM CLIN ICAL OBSERVATION TO MOLECULAR-BIOLOGY, Bulletin de la Societe de pathologie exotique et de ses filiales, 86(5), 1993, pp. 313-326
Risultati: 1-11 |