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Results: 1-18 |
Results: 18
TOWARDS A MULTIGENETIC PREDICTIVE MODEL FOR BONE-DENSITY IN HEALTHY, PREPUBERTAL GIRLS
Authors: VANTORNOUT JM SAINZ J GILSANZ V
Citation: Jm. Vantornout et al., TOWARDS A MULTIGENETIC PREDICTIVE MODEL FOR BONE-DENSITY IN HEALTHY, PREPUBERTAL GIRLS, Journal of bone and mineral research, 12, 1997, pp. 557-557
VITAMIN-D-RECEPTOR GENE POLYMORPHISMS AND BONE-DENSITY IN PREPUBERTALAMERICAN GIRLS OF MEXICAN DESCENT
Authors: SAINZ J VANTORNOUT JM LORO ML SAYRE J ROE TF GILSANZ V
Citation: J. Sainz et al., VITAMIN-D-RECEPTOR GENE POLYMORPHISMS AND BONE-DENSITY IN PREPUBERTALAMERICAN GIRLS OF MEXICAN DESCENT, The New England journal of medicine, 337(2), 1997, pp. 77-82
LAFORA PROGRESSIVE MYOCLONUS EPILEPSY - NARROWING THE CHROMOSOME 6Q24LOCUS BY RECOMBINATIONS AND HOMOZYGOSITIES
Authors: SAINZ J MINASSIAN BA SERRATOSA JM GEE MN SAKAMOTO LM IRANMANESH R BOHLEGA S BAUMANN RJ RYAN S SPARKES RS DELGADOESCUETA AV
Citation: J. Sainz et al., LAFORA PROGRESSIVE MYOCLONUS EPILEPSY - NARROWING THE CHROMOSOME 6Q24LOCUS BY RECOMBINATIONS AND HOMOZYGOSITIES, American journal of human genetics, 61(5), 1997, pp. 1205-1209
COLLAGEN TYPE-1 ALPHA-1 GENE POLYMORPHISM ASSOCIATED WITH LOW BONE-DENSITY IN PREPUBERTAL GIRLS
Authors: SAINZ J VANTOURNOUT J GILSANZ V
Citation: J. Sainz et al., COLLAGEN TYPE-1 ALPHA-1 GENE POLYMORPHISM ASSOCIATED WITH LOW BONE-DENSITY IN PREPUBERTAL GIRLS, American journal of human genetics, 61(4), 1997, pp. 214-214
RELATIONSHIP BETWEEN VITAMIN-D-RECEPTOR ALLELES AND THE VOLUME AND DENSITY OF CORTICAL BONE IN CHILDREN
Authors: KOVANLIKAVA A SAINZ J LORO ML SAYRE J ROE T GILSANZ V
Citation: A. Kovanlikava et al., RELATIONSHIP BETWEEN VITAMIN-D-RECEPTOR ALLELES AND THE VOLUME AND DENSITY OF CORTICAL BONE IN CHILDREN, Journal of bone and mineral research, 11, 1996, pp. 475-475
IDENTIFICATION OF 3 NEUROFIBROMATOSIS TYPE-2 (NF2) GENE-MUTATIONS IN VESTIBULAR SCHWANNOMAS
Authors: SAINZ J FIGUEROA K BASER ME PULST SM
Citation: J. Sainz et al., IDENTIFICATION OF 3 NEUROFIBROMATOSIS TYPE-2 (NF2) GENE-MUTATIONS IN VESTIBULAR SCHWANNOMAS, Human genetics, 97(1), 1996, pp. 121-123
PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS
Authors: BASER ME MAUTNER VF RAGGE NK NECHIPORUK A RICCARDI VM KLEIN J SAINZ J PULST SM
Citation: Me. Baser et al., PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS, Neurology, 47(5), 1996, pp. 1269-1277
GENETICS OF MYOCLONIC AND MYOCLONUS EPILEPSIES
Authors: MINASSIAN BA SAINZ J DELGADOESCUETA AV
Citation: Ba. Minassian et al., GENETICS OF MYOCLONIC AND MYOCLONUS EPILEPSIES, Clinical neuroscience, 3(4), 1995, pp. 223-235
CONSTRUCTION AND UTILITY OF A HUMAN-CHROMOSOME 22-SPECIFIC FOSMID LIBRARY
Authors: KIM UJ SHIZUYA H SAINZ J GARNES J PULST SM DEJONG P SIMON MI
Citation: Uj. Kim et al., CONSTRUCTION AND UTILITY OF A HUMAN-CHROMOSOME 22-SPECIFIC FOSMID LIBRARY, GENET A-BIO, 12(2), 1995, pp. 81-84
HIGH-FREQUENCY OF NONSENSE MUTATIONS IN THE NF2 GENE CAUSED BY C TO TTRANSITIONS IN 5 CGA CODONS
Authors: SAINZ J FIGUEROA K BASER ME MAUTNER VF PULST SM
Citation: J. Sainz et al., HIGH-FREQUENCY OF NONSENSE MUTATIONS IN THE NF2 GENE CAUSED BY C TO TTRANSITIONS IN 5 CGA CODONS, Human molecular genetics, 4(1), 1995, pp. 137-139
OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2
Authors: RAGGE NK BASER ME KLEIN J NECHIPORUK A SAINZ J PULST SM RICCARDI VM
Citation: Nk. Ragge et al., OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2, American journal of ophthalmology, 120(5), 1995, pp. 634-641
CONSTRUCTION OF A 7 CM YAC CONTIG WITHIN THE REGION OF THE JUVENILE MYOCLONIC EPILEPSY GENE ON CHROMOSOME 6P12-P11
Authors: SAINZ J SERRATOSA JM SHIH S DELGADOESCUETA AV
Citation: J. Sainz et al., CONSTRUCTION OF A 7 CM YAC CONTIG WITHIN THE REGION OF THE JUVENILE MYOCLONIC EPILEPSY GENE ON CHROMOSOME 6P12-P11, American journal of human genetics, 57(4), 1995, pp. 1563-1563
MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS
Authors: SAINZ J HUYNH DP FIGUEROA K RAGGE NK BASER ME PULST SM
Citation: J. Sainz et al., MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS, Human molecular genetics, 3(6), 1994, pp. 885-891
CA-REPEAT POLYMORPHISM AT THE D22S430 LOCUS ADJACENT TO NF2
Authors: SAINZ J NECHIPORUK A KIM UJ SIMON MI PULST SM
Citation: J. Sainz et al., CA-REPEAT POLYMORPHISM AT THE D22S430 LOCUS ADJACENT TO NF2, Human molecular genetics, 2(12), 1993, pp. 2203-2203
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D22S351 LOCUS
Authors: SAINZ J RASMUSSEN M NECHIPORUK A VISSING H CHENG X KORENBERG JR PULST SM
Citation: J. Sainz et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D22S351 LOCUS, Human molecular genetics, 2(10), 1993, pp. 1749-1749
LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22
Authors: SAINZ J BASER ME RAGGE NK NELSON RA PULST SM
Citation: J. Sainz et al., LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22, Archives of otolaryngology, head & neck surgery, 119(12), 1993, pp. 1285-1288
MUTATIONS IN THE NEUROFIBROMATOSIS-2 GENE IN 31 VESTIBULAR SCHWANNOMAS
Authors: SAINZ J FIGUEROA C BASER ME PULAT SM
Citation: J. Sainz et al., MUTATIONS IN THE NEUROFIBROMATOSIS-2 GENE IN 31 VESTIBULAR SCHWANNOMAS, American journal of human genetics, 53(3), 1993, pp. 354-354
PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS
Authors: PULST SM BASER ME MAUTNER V SAINZ J NECHIPORUK A KLEIN J NELSON RA RAGGE NK RICCARDI VM
Citation: Sm. Pulst et al., PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS, American journal of human genetics, 53(3), 1993, pp. 488-488
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