ACNP - Italian Periodicals Catalogue

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Results: 1-23 |

Results: 23

DETERMINATION OF DIESEL GENOTOXICITY IN FIREBREATHERS BY MICRONUCLEI AND NUCLEAR ABNORMALITIES IN BUCCAL MUCOSA

Authors: TORRESBUGARIN O ANDACASILLAS AD RAMIREZMUNOZ MP SANCHEZCORONA J CANTU JM ZUNIGA G

Citation: O. Torresbugarin et al., DETERMINATION OF DIESEL GENOTOXICITY IN FIREBREATHERS BY MICRONUCLEI AND NUCLEAR ABNORMALITIES IN BUCCAL MUCOSA, Mutation research. Genetic toxicology and environmental mutagenesis, 413(3), 1998, pp. 277-281

HETEROALLELIC MONOZYGOTIC TWINS AND TRIPLETS

Authors: CANTU JM DIAZGALLARDO MY BARROSNUNEZ P FIGUERA LE

Citation: Jm. Cantu et al., HETEROALLELIC MONOZYGOTIC TWINS AND TRIPLETS, American journal of medical genetics, 77(2), 1998, pp. 166-167

A NOVEL LEU171PRO MUTATION IN PRESENILIN-1 GENE IN A MEXICAN FAMILY WITH EARLY-ONSET ALZHEIMER-DISEASE

Authors: RAMIREZDUENAS MG ROGAEVA EA LEAL CA LIN C RAMIREZCASILLAS GA HERNANDEZROMO JA STGEORGEHYSLOP PH CANTU JM

Citation: Mg. Ramirezduenas et al., A NOVEL LEU171PRO MUTATION IN PRESENILIN-1 GENE IN A MEXICAN FAMILY WITH EARLY-ONSET ALZHEIMER-DISEASE, Annales de genetique, 41(3), 1998, pp. 149-153

THE GLOBALIZATION OF ETHICS - A LONG WAY TO GO

Authors: CANTU JM

Citation: Jm. Cantu, THE GLOBALIZATION OF ETHICS - A LONG WAY TO GO, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 67-67

ANALYSIS OF 16 CYSTIC-FIBROSIS MUTATIONS IN MEXICAN PATIENTS

Authors: VILLALOBOSTORRES C ROJASMARTINEZ A VILLAREALCASTELLANOS E CANTU JM SANCHEZANZALDO FJ SAIKI RK BARRERASALDANA HA

Citation: C. Villalobostorres et al., ANALYSIS OF 16 CYSTIC-FIBROSIS MUTATIONS IN MEXICAN PATIENTS, American journal of medical genetics, 69(4), 1997, pp. 380-382

CONGENITAL HYPERTRICHOSIS, OSTEOCHONDRODYSPLASIA, AND CARDIOMEGALY - FURTHER DELINEATION OF A NEW GENETIC SYNDROME

Authors: GARCIACRUZ D SANCHEZCORONA J NAZARA Z GARCIACRUZ MO FIGUERA LE CASTANEDA V CANTU JM

Citation: D. Garciacruz et al., CONGENITAL HYPERTRICHOSIS, OSTEOCHONDRODYSPLASIA, AND CARDIOMEGALY - FURTHER DELINEATION OF A NEW GENETIC SYNDROME, American journal of medical genetics, 69(2), 1997, pp. 138-151

SPONTANEOUS MICRONUCLEI IN PERIPHERAL-BLOOD ERYTHROCYTES FROM 35 MAMMALIAN-SPECIES

Authors: ZUNIGA G TORRESBUGARIN O RAMIREZMUNOZ MP RAMOS A FANTIRODRIGUEZ E PORTILLA E GARCIAMARTINEZ D CANTU JM GALLEGOSARREOLA MP SANCHEZCORONA J

Citation: G. Zuniga et al., SPONTANEOUS MICRONUCLEI IN PERIPHERAL-BLOOD ERYTHROCYTES FROM 35 MAMMALIAN-SPECIES, Mutation research. Genetic toxicology testing, 369(1-2), 1996, pp. 123-127

MICRONUCLEATED ERYTHROCYTES IN SPLENECTOMIZED PATIENTS WITH AND WITHOUT CHEMOTHERAPY

Authors: ZUNIGA G TORRESBUGARIN O RAMIREZMUNOZ MP DELGADOLAMAS JL DELOZASALDANA R CANTU JM

Citation: G. Zuniga et al., MICRONUCLEATED ERYTHROCYTES IN SPLENECTOMIZED PATIENTS WITH AND WITHOUT CHEMOTHERAPY, Mutation research. Section on environmental mutagenesis and related subjects, 361(2-3), 1996, pp. 107-112

MAPPING OF THE CONGENITAL GENERALIZED HYPERTRICHOSIS LOCUS TO CHROMOSOME XQ24-Q27.1

Authors: FIGUERA LE PANDOLFO M DUNNE PW CANTU JM PATEL PI

Citation: Le. Figuera et al., MAPPING OF THE CONGENITAL GENERALIZED HYPERTRICHOSIS LOCUS TO CHROMOSOME XQ24-Q27.1, Nature genetics, 10(2), 1995, pp. 202-207

MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION

Authors: DIAZGALLARDO MY BARROSNUNEZ P DIAZ CA HERNANDEZ A GOMEZESPINEL I LEAL CA FRAGOSO R FIGUERA L GARCIACRUZ D RAMIREZDUENAS ML CANTU JM

Citation: My. Diazgallardo et al., MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION, Archives of medical research, 26, 1995, pp. 77-83

ARE THE FACIOTHORACOSKELETAL SYNDROME AND THE GUADALAJARA CAMPTODACTYLY SYNDROME TYPE-I DISTINCT ENTITIES

Authors: RAMIREZDUENAS ML CANTU JM

Citation: Ml. Ramirezduenas et Jm. Cantu, ARE THE FACIOTHORACOSKELETAL SYNDROME AND THE GUADALAJARA CAMPTODACTYLY SYNDROME TYPE-I DISTINCT ENTITIES, American journal of medical genetics, 58(3), 1995, pp. 293-293

CHRISTIANS SPONDYLO-DIGITAL-SYNDROME - 2ND FAMILIAL CASE

Authors: GARCIACRUZ D CANTU JM GARCIAMARTINEZ FJ GARCIACRUZ WO NAZARA Z GONZALEZULLOA B HERNANDEZCORDOVA A RUIZ MX SANCHEZCORONA J

Citation: D. Garciacruz et al., CHRISTIANS SPONDYLO-DIGITAL-SYNDROME - 2ND FAMILIAL CASE, Clinical genetics, 48(5), 1995, pp. 268-271

SPONDYLO-CAMPTODACTYLY SYNDROME - A DISTINCT AUTOSOMAL-DOMINANT ENTITY

Authors: LIZCANOGIL LA GARCIACRUZ D SANCHEZCORONA J CANTU JM

Citation: La. Lizcanogil et al., SPONDYLO-CAMPTODACTYLY SYNDROME - A DISTINCT AUTOSOMAL-DOMINANT ENTITY, Clinical genetics, 48(4), 1995, pp. 173-176

PARENTAL ORIGIN OF THE EXTRA CHROMOSOMES IN POLYSOMY-X

Authors: LEAL CA BELMONT JW NACHTMAN R CANTU JM MEDINA C

Citation: Ca. Leal et al., PARENTAL ORIGIN OF THE EXTRA CHROMOSOMES IN POLYSOMY-X, Human genetics, 94(4), 1994, pp. 423-426

SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) SHOHAT TYPE

Authors: FIGUERA LE RAMIREZDUENAS ML GALLEGOSARREOLA MP CANTU JM

Citation: Le. Figuera et al., SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) SHOHAT TYPE, American journal of medical genetics, 51(3), 1994, pp. 213-215

AMBRAL SYNDROME AND CONGENITAL GENERALIZED HYPERTRICHOSIS

Authors: FIGUERA LE CANTU JM

Citation: Le. Figuera et Jm. Cantu, AMBRAL SYNDROME AND CONGENITAL GENERALIZED HYPERTRICHOSIS, Clinical genetics, 46(5), 1994, pp. 384-384

PSYCHOMETRIC ANALYSIS IN CHILDREN WITH MENTAL-RETARDATION DUE TO PERINATAL HYPOXIA TREATED WITH FIBROBLAST GROWTH-FACTOR (FGF) AND SHOWING IMPROVEMENT IN MENTAL-DEVELOPMENT

Authors: AGUILAR LC ISLAS A ROSIQUE P HERNANDEZ B PORTILLO E HERRERA JM CORTES R CRUZ S ALFARO F MARTIN R CANTU JM

Citation: Lc. Aguilar et al., PSYCHOMETRIC ANALYSIS IN CHILDREN WITH MENTAL-RETARDATION DUE TO PERINATAL HYPOXIA TREATED WITH FIBROBLAST GROWTH-FACTOR (FGF) AND SHOWING IMPROVEMENT IN MENTAL-DEVELOPMENT, JIDR. Journal of intellectual disability research, 37, 1993, pp. 507-520

SCHWARTZ-JAMPEL SYNDROME - AN ATYPICAL FORM

Authors: FIGUERA LE JIMENEZGIL FJ GARCIACRUZ MO CANTU JM

Citation: Le. Figuera et al., SCHWARTZ-JAMPEL SYNDROME - AN ATYPICAL FORM, American journal of medical genetics, 47(4), 1993, pp. 526-528

ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA - A NEW VARIANT

Authors: FIGUERA LE RIVAS F CANTU JM

Citation: Le. Figuera et al., ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA - A NEW VARIANT, Clinical genetics, 44(4), 1993, pp. 190-192

THE MYHRE SYNDROME - REPORT OF 2 CASES

Authors: GARCIACRUZ D FIGUERA LE FERIAVELAZCO A SANCHEZCORONA J GARCIACRUZ MO RAMIREZDUENAS RM HERNANDEZCORDOVA A RUIZ MX BITARALATORRE WE RAMIREZDUENAS ML CANTU JM

Citation: D. Garciacruz et al., THE MYHRE SYNDROME - REPORT OF 2 CASES, Clinical genetics, 44(4), 1993, pp. 203-207

KAUFMAN OCULOCEREBROFACIAL SYNDROME - REPORT OF 2 NEW CASES AND FURTHER DELINEATION

Authors: FIGUERA LE GARCIACRUZ D RAMIREZUENAS ML RIVERAROBLES V CANTU JM

Citation: Le. Figuera et al., KAUFMAN OCULOCEREBROFACIAL SYNDROME - REPORT OF 2 NEW CASES AND FURTHER DELINEATION, Clinical genetics, 44(2), 1993, pp. 98-101

TRANSLOCATION 43 WITH ADJACENT 1 AND 3-1 SEGREGATIONS LEADING TO COMPLEMENTARY SEGMENTAL TRISOMIES 13

Authors: BARROSNUNEZ P HIGAREDA O CANTU JM

Citation: P. Barrosnunez et al., TRANSLOCATION 43 WITH ADJACENT 1 AND 3-1 SEGREGATIONS LEADING TO COMPLEMENTARY SEGMENTAL TRISOMIES 13, Annales de genetique, 36(3), 1993, pp. 176-180

GUADALAJARA CAMPTODACTYLY SYNDROME TYPE-III

Authors: FIGUERA LE RAMIREZDUENAS M CANTU JM

Citation: Le. Figuera et al., GUADALAJARA CAMPTODACTYLY SYNDROME TYPE-III, American journal of human genetics, 53(3), 1993, pp. 429-429

Risultati: 1-23 |