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Results: 16
GENETIC-ANALYSIS OF A FAMILY WITH X-LINKED MENTAL-RETARDATION, HYPOGONADISM AND RETINITIS-PIGMENTOSA
Authors:
MILLAN JM
MARTINEZ F
RAMOS MA
PRIETO F
Citation: Jm. Millan et al., GENETIC-ANALYSIS OF A FAMILY WITH X-LINKED MENTAL-RETARDATION, HYPOGONADISM AND RETINITIS-PIGMENTOSA, European journal of human genetics, 6, 1998, pp. 4007-4007
Authors:
MARTINEZ F
MARTINEZ C
MILLAN JM
PALAU F
PRIETO F
Citation: F. Martinez et al., LOCALIZATION OF X-LINKED ARTHROGRIPOSIS TYPE-I (X-LINKED INFANTILE SPINAL ATROPHY) TO XP21-Q12 IN A NEW FAMILY, European journal of human genetics, 6, 1998, pp. 4008-4008
Authors:
ESPINOS C
MILLAN JM
SANCHEZ F
BENEYTO M
NAJERA C
Citation: C. Espinos et al., ALA397ASP MUTATION OF MYOSIN VIIA GENE SEGREGATING IN A SPANISH FAMILY WITH TYPE-1B USHER-SYNDROME, Human genetics, 102(6), 1998, pp. 691-694
Authors:
ORELLANA C
HERNANDEZMARTI M
MARTINEZ F
CASTEL V
MILLAN JM
ALVAREZGARIJO JA
PRIETO F
BADIA L
Citation: C. Orellana et al., PEDIATRIC BRAIN-TUMORS - LOSS OF HETEROZYGOSITY AT 17P AND TP53 GENE-MUTATIONS, Cancer genetics and cytogenetics, 102(2), 1998, pp. 93-99
Authors:
ESPINOS C
MILLAN JM
Citation: C. Espinos et Jm. Millan, GENETIC INVESTIGATION ON USHER-SYNDROME I N SPAIN, Medicina Clinica, 110(9), 1998, pp. 340-341
Authors:
ESPINOS C
NAJERA C
MILLAN JM
AYUSO C
BAIGET M
PEREZGARRIGUES H
RODRIGO O
VILELA C
BENEYTO M
Citation: C. Espinos et al., LINKAGE ANALYSIS IN USHER-SYNDROME TYPE-I (USH1) FAMILIES FROM SPAIN, Journal of Medical Genetics, 35(5), 1998, pp. 391-398
Authors:
MARTINEZ F
TOMAS M
MILLAN JM
FERNANDEZ A
PALAU F
PRIETO F
Citation: F. Martinez et al., GENETIC LOCALIZATION OF MENTAL-RETARDATION WITH SPASTIC DIPLEGIA TO THE PERICENTROMERIC REGION OF THE X-CHROMOSOME - X-INACTIVATION IN FEMALE CARRIERS, Journal of Medical Genetics, 35(4), 1998, pp. 284-287
Authors:
BORT S
NELIS E
TIMMERMAN V
SEVILLA T
CRUZMARTINEZ A
MARTINEZ F
MILLAN JM
ARPA J
VILCHEZ JJ
PRIETO F
VANBROECKHOVEN C
PALAU F
Citation: S. Bort et al., MUTATIONAL ANALYSIS OF THE MPZ, PMP22 AND CX32 GENES IN PATIENTS OF SPANISH ANCESTRY WITH CHARCOT-MARIE-TOOTH-DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Human genetics, 99(6), 1997, pp. 746-754
Authors:
MILLAN JM
PURDIE JL
MELVILLE LF
Citation: Jm. Millan et al., PUBLIC-HEALTH RISKS OF THE FLESH OF FARMED CROCODILES, Revue scientifique et technique - Office international des epizooties, 16(2), 1997, pp. 605-608
Authors:
BUENVIAJE GN
HIRST RG
LADDS PW
MILLAN JM
Citation: Gn. Buenviaje et al., ISOLATION OF DERMATOPHILUS SP FROM SKIN-LESIONS IN FARMED SALTWATER CROCODILES (CROCODYLUS-POROSUS), Australian Veterinary Journal, 75(5), 1997, pp. 365-367
Authors:
VILELA C
BENEYTO M
BOSCH R
MILLAN JM
MARCO M
VALLET M
ALONSO L
TORMOS I
NAJERA C
VALLS B
PARICIO N
PRIETO F
Citation: C. Vilela et al., CLINICAL AND GENETIC-ASPECTS OF 2 SPANISH FAMILIES WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (ADRP), Ophthalmic genetics, 17(1), 1996, pp. 29-33
Authors:
MILLAN JM
FUCHS S
PARICIO N
WEDEMANN H
GAL A
NAJERA C
PRIETO F
Citation: Jm. Millan et al., GLY114ASP MUTATION OF RHODOPSIN IN AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA, Molecular and cellular probes, 9(1), 1995, pp. 67-69
Authors:
NAJERA C
MILLAN JM
BENEYTO M
PRIETO F
Citation: C. Najera et al., EPIDEMIOLOGY OF RETINITIS-PIGMENTOSA IN THE VALENCIAN COMMUNITY (SPAIN), Genetic epidemiology, 12(1), 1995, pp. 37-46
Authors:
MILLAN JM
MARTINEZ F
VILELA C
BENEYTO M
PRIETO F
NAJERA C
Citation: Jm. Millan et al., AN AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA FAMILY WITH CLOSE LINKAGE TO D7S480 ON 7Q, Human genetics, 96(2), 1995, pp. 216-218
Authors:
GRUNING G
MILLAN JM
MEINS M
BENEYTO M
CABALLERO M
APFELSTEDTSYLLA E
BOSCH R
ZRENNER E
PRIETO F
GAL A
Citation: G. Gruning et al., MUTATIONS IN THE HUMAN PERIPHERIN RDS GENE ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA/, Human mutation, 3(3), 1994, pp. 321-323
Authors:
MILLAN JM
NAJERA C
BENEYTO M
Citation: Jm. Millan et al., MOLECULAR-GENETICS OF RETINITIS-PIGMENTOS A, Medicina Clinica, 102(1), 1994, pp. 30-32
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