| Missing Links?: 1046 Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 9713,
Authors: 21853,
Journals: 1676,
Outer References: 261037,
Words: 13682
Collection span: 1947 - 2005
View: Overview. Sorted by journal name.
Page 45 of 98: 1 11 21 31 [ 41 42 43 44 45 46 47 48 49 50 ] 51 61 71 81 91
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 4401 | 8 | 50 | 3477 1991 GENOMICS 11 (2): 324-333 WARBURTON PE; GREIG GM; HAAF T; WILLARD HF PCR AMPLIFICATION OF CHROMOSOME-SPECIFIC ALPHA-SATELLITE DNA - DEFINITION OF CENTROMERIC STS MARKERS AND POLYMORPHIC ANALYSIS | 4 | 61 |
| 4402 | 6 | 48 | 3478 1991 GENOMICS 11 (2): 379-388 CARSON NL; SIMPSON NE A PHYSICAL MAP OF HUMAN CHROMOSOME-10 AND A COMPARISON WITH AN EXISTING GENETIC-MAP | 1 | 13 |
| 4403 | 7 | 12 | 3479 1991 GENOMICS 11 (2): 490-491 CAVALLISFORZA LL; WILSON AC; CANTOR CR; COOKDEEGAN RM; KING MC CALL FOR A WORLDWIDE SURVEY OF HUMAN GENETIC DIVERSITY - A VANISHING OPPORTUNITY FOR THE HUMAN GENOME PROJECT | 55 | 55 |
| 4404 | 10 | 51 | 3480 1991 GENOMICS 11 (2): 491-498 BOWCOCK A; CAVALLISFORZA LL THE STUDY OF VARIATION IN THE HUMAN GENOME | 29 | 29 |
| 4405 | 16 | 56 | 3481 1991 GENOMICS 11 (3): 517-529 BOWCOCK AM; FARRER LA; HEBERT JM; BALE AE; CAVALLISFORZA LL A CONTIGUOUS LINKAGE MAP OF CHROMOSOME-13Q WITH 39 DISTINCT LOCI SEPARATED ON AVERAGE BY 5.1 CENTIMORGANS | 38 | 38 |
| 4406 | 5 | 29 | 3482 1991 GENOMICS 11 (4): 941-947 BARR FG; SELLINGER B; EMANUEL BS LOCALIZATION OF THE RHABDOMYOSARCOMA T(2-13) BREAKPOINT ON A PHYSICAL MAP OF CHROMOSOME-13 | 6 | 16 |
| 4407 | 2 | 29 | 3780 1992 GENOMICS 12 (1): 130-138 VETRIE D; FLINTER F; BOBROW M; HARRIS A LONG-RANGE MAPPING OF THE GENE FOR THE HUMAN ALPHA-5(IV) COLLAGEN CHAIN AT XQ22-Q23 | 2 | 14 |
| 4408 | 6 | 21 | 3781 1992 GENOMICS 12 (2): 276-280 KRETZ KA; CRIPE D; CARSON GS; FUKUSHIMA H; OBRIEN JS STRUCTURE AND SEQUENCE OF THE HUMAN ALPHA-L-FUCOSIDASE GENE AND PSEUDOGENE | 9 | 24 |
| 4409 | 2 | 67 | 3782 1992 GENOMICS 12 (2): 388-393 MOORE KJ; DAMOREBRUNO MA; KORFHAGEN TR; GLASSER SW; WHITSETT JA; et al. CHROMOSOMAL LOCALIZATION OF 3 PULMONARY SURFACTANT PROTEIN GENES IN THE MOUSE | 4 | 38 |
| 4410 | 3 | 28 | 3783 1992 GENOMICS 12 (3): 430-434 ALBRITTON LM; BOWCOCK AM; EDDY RL; MORTON CC; TSENG L; et al. THE HUMAN CATIONIC AMINO-ACID TRANSPORTER (ATRC1) - PHYSICAL AND GENETIC-MAPPING TO 13Q12-Q14 | 35 | 35 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4411 | 1 | 19 | 3784 1992 GENOMICS 13 (1): 89-94 HEDING IJJP; IVENS AC; WILSON J; STRIVENS M; GREGORY S; et al. THE GENERATION OF ORDERED SETS OF COSMID DNA CLONES FROM HUMAN-CHROMOSOME REGION-11P | 0 | 16 |
| 4412 | 5 | 29 | 3785 1992 GENOMICS 13 (1): 104-108 MOXLEY G; GIBBS RS POLYMERASE CHAIN REACTION-BASED GENOTYPING FOR ALLOTYPIC MARKERS OF IMMUNOGLOBULIN KAPPA-SHOWS ALLELIC ASSOCIATION OF KM WITH KAPPA-VARIABLE SEGMENT | 5 | 23 |
| 4413 | 5 | 23 | 3786 1992 GENOMICS 13 (1): 189-193 BROWN KA; SUTCLIFFE MJ; STEEL KP; BROWN SDM CLOSE LINKAGE OF THE OLFACTORY MARKER PROTEIN GENE TO THE MOUSE DEAFNESS MUTATION SHAKER-1 | 1 | 27 |
| 4414 | 2 | 20 | 3787 1992 GENOMICS 13 (3): 809-813 MARIYAMA M; ZHENG KG; YANGFENG TL; REEDERS ST COLOCALIZATION OF THE GENES FOR THE ALPHA-3(IV) AND ALPHA-4(IV) CHAINS OF TYPE-IV COLLAGEN TO CHROMOSOME-2 BANDS-Q35-Q37 | 1 | 72 |
| 4415 | 2 | 21 | 3788 1992 GENOMICS 13 (3): 852-855 CARSON WJ; RADVANY J; FARRER LA; VINCENT D; ROSENBERG RN; et al. THE MACHADO-JOSEPH DISEASE LOCUS IS DIFFERENT FROM THE SPINOCEREBELLAR ATAXIA LOCUS (SCA1) | 1 | 17 |
| 4416 | 1 | 53 | 3789 1992 GENOMICS 13 (4): 1065-1074 THALER DS; NOORDEWIER MO MEPS PARAMETERS AND GRAPH ANALYSIS FOR THE USE OF RECOMBINATION TO CONSTRUCT ORDERED SETS OF OVERLAPPING CLONES | 0 | 2 |
| 4417 | 7 | 49 | 3790 1992 GENOMICS 14 (1): 105-112 FOUNTAIN JW; KARAYIORGOU M; TARUSCIO D; GRAW SL; BUCKLER AJ; et al. GENETIC AND PHYSICAL MAP OF THE INTERFERON REGION ON CHROMOSOME-9P | 5 | 46 |
| 4418 | 3 | 25 | 3791 1992 GENOMICS 14 (2): 398-402 BOWCOCK AM; AZUMA T; BARNES RI; WU SH; BELL GI; et al. DETECTION OF A POLYMORPHISM WITHIN THE PEPSINOGEN-C GENE WITH PCR - CONSTRUCTION OF A LINKAGE MAP AROUND PGC FROM 6P11-6P21.3 | 0 | 4 |
| 4419 | 2 | 6 | 3792 1992 GENOMICS 14 (2): 550-551 KENNERKNECHT I; KLETT C; HAMEISTER H ASSIGNMENT OF THE HUMAN GENE PROPIONYL COENZYME-A CARBOXYLASE, ALPHA-CHAIN, (PCCA) TO CHROMOSOME 13Q32 BY INSITU HYBRIDIZATION | 1 | 6 |
| 4420 | 3 | 27 | 3793 1992 GENOMICS 14 (3): 590-597 EDWARDS MC; GIBBS RA A HUMAN DIMORPHISM RESULTING FROM LOSS OF AN ALU | 9 | 35 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4421 | 5 | 60 | 3794 1992 GENOMICS 14 (4): 833-840 BOWCOCK AM; BARNES RI; WHITE RL; KRUSE TA; TSIPOURAS P; et al. THE CEPH CONSORTIUM LINKAGE MAP OF HUMAN CHROMOSOME-15Q | 5 | 15 |
| 4422 | 3 | 40 | 3795 1992 GENOMICS 14 (4): 1010-1018 EUBANKS JH; DJABALI M; SELLERI L; GRANDY DK; CIVELLI O; et al. STRUCTURE AND LINKAGE OF THE D2 DOPAMINE RECEPTOR AND NEURAL CELL-ADHESION MOLECULE GENES ON HUMAN CHROMOSOME-11Q23 | 5 | 38 |
| 4423 | 2 | 19 | 4112 1993 GENOMICS 15 (1): 9-12 AHMAD F; DAVIS MB; WADDY HM; OLEY CA; MARSDEN CD; et al. EVIDENCE FOR LOCUS HETEROGENEITY IN AUTOSOMAL DOMINANT TORSION DYSTONIA | 1 | 26 |
| 4424 | 9 | 41 | 4113 1993 GENOMICS 15 (1): 76-85 PETRUKHIN KE; SPEER MC; CAYANIS E; BONALDO MD; TANTRAVAHI U; et al. A MICROSATELLITE GENETIC-LINKAGE MAP OF HUMAN CHROMOSOME-13 | 16 | 52 |
| 4425 | 1 | 27 | 4114 1993 GENOMICS 15 (1): 86-90 YUZBASIYANGURKAN V; WAGNITZ S; BLANTON SH; BREWER GJ LINKAGE STUDIES OF THE ESTERASE-D AND RETINOBLASTOMA GENES TO CANINE COPPER TOXICOSIS - A MODEL FOR WILSON DISEASE | 3 | 12 |
| 4426 | 5 | 35 | 4115 1993 GENOMICS 15 (2): 376-386 BOWCOCK A; OSBORNELAWRENCE S; BARNES R; CHAKRAVARTI A; WASHI; et al. MICROSATELLITE POLYMORPHISM LINKAGE MAP OF HUMAN CHROMOSOME-13Q | 18 | 62 |
| 4427 | 0 | 34 | 4116 1993 GENOMICS 16 (1): 69-77 KURTH JH; MOUNTAIN JL; CAVALLISFORZA LL SUBCLUSTERING OF HUMAN IMMUNOGLOBULIN-KAPPA LIGHT CHAIN VARIABLE REGION GENES | 7 | 7 |
| 4428 | 4 | 18 | 4117 1993 GENOMICS 16 (2): 355-360 WARBURTON D; YU MT; TANTRAVAHI U; LEE C; CAYANIS E; et al. REGIONAL LOCALIZATION OF 32 NOTI-HINDIII FRAGMENTS FROM A HUMAN CHROMOSOME-13 LIBRARY BY A SOMATIC-CELL HYBRID PANEL AND INSITU HYBRIDIZATION | 3 | 11 |
| 4429 | 4 | 30 | 4118 1993 GENOMICS 16 (2): 426-430 RAO PH; MURTY VVVS; GAIDANO G; HAUPTSCHEIN R; DALLAFAVERA R; et al. SUBREGIONAL LOCALIZATION OF 20 SINGLE-COPY LOCI TO CHROMOSOME-6 BY FLUORESCENCE INSITU HYBRIDIZATION | 0 | 27 |
| 4430 | 17 | 74 | 4119 1993 GENOMICS 16 (2): 486-496 BOWCOCK AM; GERKEN SC; BARNES RI; SHIANG R; JABS EW; et al. THE CEPH CONSORTIUM LINKAGE MAP OF HUMAN CHROMOSOME-13 | 14 | 14 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4431 | 4 | 13 | 4120 1993 GENOMICS 16 (2): 515-519 GERKEN S; LEPPERT M; OCONNELL P; CAVENEE W; JAMES CD; et al. A GENETIC-LINKAGE MAP WITH 29 LOCI SPANNING HUMAN CHROMOSOME-13Q | 4 | 5 |
| 4432 | 6 | 19 | 4121 1993 GENOMICS 16 (3): 593-598 BULL PC; COX DW LONG-RANGE RESTRICTION MAPPING OF 13Q14.3 FOCUSED ON THE WILSON DISEASE REGION | 6 | 7 |
| 4433 | 3 | 24 | 4122 1993 GENOMICS 16 (3): 751-754 WITKE WF; GIBBS PEM; ZIELINSKI R; YANG FM; BOWMAN BH; et al. COMPLETE STRUCTURE OF THE HUMAN GC GENE - DIFFERENCES AND SIMILARITIES BETWEEN MEMBERS OF THE ALBUMIN GENE FAMILY | 3 | 19 |
| 4434 | 3 | 44 | 4123 1993 GENOMICS 17 (1): 6-14 FILOSA S; CALABRO V; LANIA G; VULLIAMY TJ; BRANCATI C; et al. G6PD HAPLOTYPES SPANNING XQ28 FROM F8C TO RED-GREEN COLOR-VISION | 0 | 26 |
| 4435 | 1 | 65 | 4124 1993 GENOMICS 17 (1): 15-24 WARD JRT; COTTRELL S; THOMAS HJW; JONES TA; HOWE CM; et al. A LONG-RANGE RESTRICTION MAP OF HUMAN CHROMOSOME-5Q21-Q23 | 0 | 8 |
| 4436 | 30 | 122 | 4125 1993 GENOMICS 17 (1): 171-184 SHOFFNER JM; BROWN MD; TORRONI A; LOTT MT; CABELL MF; et al. MITOCHONDRIAL-DNA VARIANTS OBSERVED IN ALZHEIMER-DISEASE AND PARKINSON DISEASE PATIENTS | 11 | 231 |
| 4437 | 2 | 15 | 4126 1993 GENOMICS 17 (2): 522-524 KELSELL DP; BLACK DM; SOLOMON E; SPURR NK LOCALIZATION OF A 2ND NM23 GENE, NME2, TO CHROMOSOME-17Q21-Q22 | 0 | 11 |
| 4438 | 3 | 37 | 4127 1993 GENOMICS 17 (3): 535-543 TOGUCHIDA J; MCGEE TL; PATERSON JC; EAGLE JR; TUCKER S; et al. COMPLETE GENOMIC SEQUENCE OF THE HUMAN RETINOBLASTOMA SUSCEPTIBILITY GENE | 4 | 111 |
| 4439 | 1 | 10 | 4128 1993 GENOMICS 18 (1): 141-143 MICHALSKI AJ; COWELL JK ASSIGNMENT OF 4 SEQUENCE-TAGGED SITES TO 3 SUBREGIONS OF 13Q12 USING A SOMATIC-CELL HYBRID MAPPING PANEL | 4 | 8 |
| 4440 | 7 | 41 | 4129 1993 GENOMICS 18 (3): 486-495 WASHINGTON SS; BOWCOCK AM; GERKEN S; MATSUNAMI N; LESH D; et al. A SOMATIC-CELL HYBRID MAP OF HUMAN-CHROMOSOME-13 | 6 | 10 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4441 | 3 | 22 | 4130 1993 GENOMICS 18 (3): 598-601 BARENDSE W; ARMITAGE SM; KIRKPATRICK BW; MOORE SS; GEORGES M; et al. A GENETIC-MAP OF INDEX DNA LOCI ON BOVINE CHROMOSOME-21 | 0 | 6 |
| 4442 | 5 | 65 | 4460 1994 GENOMICS 19 (1): 12-20 SUAREZ BK; PARSIAN A; HAMPE CL; TODD RD; REICH T; et al. LINKAGE DISEQUILIBRIA AT THE D-2 DOPAMINE-RECEPTOR LOCUS (DRD2) IN ALCOHOLICS AND CONTROLS | 8 | 86 |
| 4443 | 2 | 44 | 4461 1994 GENOMICS 19 (1): 31-37 PEDEUTOUR F; SZPIRER C; NAHON JL ASSIGNMENT OF THE HUMAN PRO-MELANIN-CONCENTRATING HORMONE GENE (PMCH) TO CHROMOSOME 12Q23-Q24 AND 2 VARIANT GENES (PMCHL1 AND PMCHL2) TO CHROMOSOME 5P14 AND 5Q12-Q13 | 0 | 23 |
| 4444 | 2 | 53 | 4462 1994 GENOMICS 19 (3): 532-541 WEIFFENBACH B; DUBOIS J; MANNING S; MA NS; SCHUTTE BC; et al. YAC CONTIGS FOR 4Q35 IN THE REGION OF THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) GENE | 0 | 2 |
| 4445 | 1 | 16 | 4463 1994 GENOMICS 21 (1): 138-143 LARGETPIET D; GERBER S; BONNEAU D; ROZET JM; MARC S; et al. GENETIC-HETEROGENEITY OF USHER SYNDROME TYPE-1 IN FRENCH FAMILIES | 1 | 29 |
| 4446 | 2 | 12 | 4464 1994 GENOMICS 21 (1): 248-250 HAWTHORN L; NIZETIC D; LEHRACH H; COWELL JK ASSIGNMENT OF 55 NOVEL COSMIDS TO 7 SUBREGIONS OF CHROMOSOME-13 USING FLUORESCENCE IN SITE HYBRIDIZATION | 2 | 6 |
| 4447 | 3 | 15 | 4465 1994 GENOMICS 21 (1): 293-296 STURM RA; BAKER E; SUTHERLAND GR ASSIGNMENT OF THE TYROSINASE-RELATED PROTEIN-2 GENE (TYRPZ) TO HUMAN-CHROMOSOME 13Q31-Q32 BY FLUORESCENCE IN-SITU HYBRIDIZATION - EXTENDED SYNTENY WITH MOUSE CHROMOSOME-14 | 0 | 11 |
| 4448 | 1 | 59 | 4466 1994 GENOMICS 22 (1): 137-147 SELLERI L; GIOVANNINI M; HERMANSON GG; ROMO A; QUACKENBUSH J; et al. YEAST ARTIFICIAL CHROMOSOME CLONING OF 3.2 MEGABASES WITHIN CHROMOSOMAL BAND-11Q24 CLOSELY LINKING C-ETS-1 AND FLI-1 AND ENCOMPASSING THE EWING-SARCOMA BREAKPOINT | 0 | 12 |
| 4449 | 1 | 28 | 4467 1994 GENOMICS 22 (3): 637-640 LEVY FO; HOLTGREVEGREZ H; TASKEN K; SOLBERG R; RIED T; et al. ASSIGNMENT OF THE GENE ENCODING THE 5-HT1E SEROTONIN RECEPTOR (S31) (LOCUS HTR1E) TO HUMAN-CHROMOSOME 6Q14-Q15 | 2 | 9 |
| 4450 | 2 | 18 | 4468 1994 GENOMICS 23 (1): 138-144 KWOK PY; CARLSON C; YAGER TD; ANKENER W; NICKERSON DA COMPARATIVE-ANALYSIS OF HUMAN DNA VARIATIONS BY FLUORESCENCE-BASED SEQUENCING OF PCR PRODUCTS | 13 | 83 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4451 | 3 | 35 | 4469 1994 GENOMICS 23 (2): 331-337 COX DW; BILLINGSLEY G; NGUYEN VTT A LINKAGE MAP OF HUMAN-CHROMOSOME-14, INCLUDING 13 GENE LOCI | 1 | 11 |
| 4452 | 1 | 42 | 4470 1994 GENOMICS 23 (3): 582-& BRANDRIFF BF; GORDON LA; FERTITTA A; OLSEN AS; CHRISTENSEN M; et al. HUMAN-CHROMOSOME-19P - A FLUORESCENCE IN-SITU HYBRIDIZATION MAP WITH GENOMIC DISTANCE ESTIMATES FOR 79 INTERVALS SPANNING 20-MB | 0 | 52 |
| 4453 | 4 | 38 | 4816 1995 GENOMICS 25 (1): 44-58 KOZMAN HM; KEITH TP; DONISKELLER H; WHITE RL; WEISSENBACH J; et al. THE CEPH CONSORTIUM LINKAGE MAP OF HUMAN-CHROMOSOME-16 | 1 | 19 |
| 4454 | 4 | 36 | 4817 1995 GENOMICS 27 (1): 101-112 LITT M; KRAMER P; KORT E; FAIN P; COX S; et al. THE CEPH CONSORTIUM LINKAGE MAP OF HUMAN-CHROMOSOME-11 | 4 | 24 |
| 4455 | 9 | 29 | 4818 1995 GENOMICS 27 (3): 399-404 HAWTHORN L; COWELL JK INTEGRATION OF THE PHYSICAL AND GENETIC-LINKAGE MAP FOR HUMAN-CHROMOSOME-13 | 5 | 15 |
| 4456 | 11 | 55 | 4819 1995 GENOMICS 27 (3): 502-510 SHAW SH; FARR JEW; THIEL BA; MATISE TC; WEISSENBACH J; et al. A RADIATION HYBRID MAP OF 95-STSS SPANNING HUMAN-CHROMOSOME 13Q | 3 | 15 |
| 4457 | 5 | 45 | 4820 1995 GENOMICS 28 (2): 131-139 IBBERSON MR; COPIER JP; SO AK GENOMIC ORGANIZATION OF THE HUMAN T-CELL RECEPTOR VARIABLE-ALPHA (TCRAV) GENE-CLUSTER | 2 | 11 |
| 4458 | 8 | 56 | 4821 1995 GENOMICS 29 (2): 311-322 DEVLIN B; RISCH N A COMPARISON OF LINKAGE DISEQUILIBRIUM MEASURES FOR FINE-SCALE MAPPING | 18 | 302 |
| 4459 | 1 | 5 | 4822 1995 GENOMICS 29 (2): 551-552 RAUCH H; WELLS AJ THE TOXIC MILK MUTATION, TX, WHICH RESULTS IN A CONDITION RESEMBLING WILSON DISEASE IN HUMANS, IS LINKED TO MOUSE CHROMOSOME-8 | 0 | 6 |
| 4460 | 7 | 26 | 4823 1995 GENOMICS 30 (3): 425-430 Hawthorn L; Roberts T; Verlind E; Kooy RF; Cowell JK A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemia | 4 | 22 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4461 | 7 | 51 | 5216 1996 GENOMICS 33 (2): 159-166 Still IH; Roberts T; Bia B; Hawthorn L; Auffray C; et al. Incorporation of 35 novel gene transcripts into the physical and genetic map of human chromosome 13 | 0 | 5 |
| 4462 | 3 | 64 | 5217 1996 GENOMICS 36 (1): 142-150 Stoilova D; Child A; Trifan OC; Crick RP; Coakes RL; et al. Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region | 0 | 85 |
| 4463 | 1 | 35 | 5616 1997 GENOMICS 39 (2): 164-170 Karrman C; Backman B; Dixon M; Holmgren G; Forsman K Mapping of the locus for autosomal dominant: Amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21 | 0 | 25 |
| 4464 | 6 | 33 | 5617 1997 GENOMICS 40 (3): 409-414 Wintle RF; Nygaard TG; Herbrick JAS; Kvaloy K; Cox DW Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q | 1 | 17 |
| 4465 | 1 | 21 | 6017 1998 GENOMICS 47 (1): 1-6 Cheung VG; Nelson SF Genomic mismatch scanning identifies human genomic DNA shared identical by descent | 0 | 17 |
| 4466 | 9 | 48 | 6018 1998 GENOMICS 47 (1): 26-43 Cayanis E; Russo JJ; Kalachikov S; Ye XL; Park SH; et al. High-resolution YAC-Cosmid-STS map of human chromosome 13 | 0 | 20 |
| 4467 | 3 | 10 | 6019 1998 GENOMICS 47 (1): 146-148 Kato MV; Ikawa Y; Hayashizaki Y; Shibata H Paternal imprinting of mouse serotonin receptor 2A gene Htr2 in embryonic eye: A conserved imprinting regulation on the RB/Rb locus | 1 | 10 |
| 4468 | 3 | 39 | 6020 1998 GENOMICS 49 (2): 230-236 Sperandeo MP; Borsani G; Incerti B; Zollo M; Rossi E; et al. The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome | 2 | 25 |
| 4469 | 3 | 23 | 6021 1998 GENOMICS 52 (1): 44-49 O'Donovan MC; Oefner PJ; Roberts SC; Austin J; Hoogendoorn B; et al. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection | 70 | 170 |
| 4470 | 8 | 24 | 6022 1998 GENOMICS 53 (1): 12-20 Morin PA; Mahboubi P; Wedel S; Rogers J Rapid screening and comparison of human microsatellite markers in baboons: Allele size is conserved, but allele number is not | 4 | 28 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4471 | 4 | 20 | 6452 1999 GENOMICS 56 (3): 247-253 Giordano M; Oefner PJ; Underhill PA; Sforza LLC; Tosi R; et al. Identification by denaturing high-performance liquid chromatography of numerous polymorphisms in a candidate region for multiple sclerosis susceptibility | 15 | 30 |
| 4472 | 4 | 14 | 6453 1999 GENOMICS 57 (3): 433-437 White PS; Tatum OL; Deaven LL; Longmire JL New, male-specific microsatellite markers from the human Y chromosome | 12 | 49 |
| 4473 | 2 | 11 | 6454 1999 GENOMICS 58 (3): 310-312 Marsh S; Collie-Duguid ESR; Li T; Liu XH; McLeod HL Ethnic variation in the thymidylate synthase enhancer region polymorphism among Caucasian and Asian populations | 0 | 49 |
| 4474 | 1 | 26 | 6455 1999 GENOMICS 58 (3): 323-326 Leonard JC; Toji LH; Bender PK; Beiswanger CM; Beck JC; et al. Regional mapping panels for chromosomes 6, 9, and 16 | 0 | 3 |
| 4475 | 7 | 22 | 6456 1999 GENOMICS 62 (3): 369-376 Wagner T; Stoppa-Lyonnet D; Fleischmann E; Muhr D; Pages S; et al. Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations | 30 | 95 |
| 4476 | 2 | 87 | 6909 2000 GENOMICS 67 (2): 109-127 Bowles KR; Abraham SE; Brugada R; Zintz C; Comeaux J; et al. Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes | 0 | 8 |
| 4477 | 4 | 28 | 6910 2000 GENOMICS 70 (2): 153-164 Escary JL; Bottius E; Prince N; Reyes C; Fiawoumo Y; et al. A first high-density map of 981 biallelic markers on human chromosome 14 | 0 | 3 |
| 4478 | 2 | 17 | 7419 2001 GENOMICS 71 (1): 118-122 Passarino G; Shen P; Van Kirk JB; Lin AA; De Benedictis G; et al. The Werner syndrome gene and global sequence variation | 4 | 6 |
| 4479 | 8 | 47 | 7420 2001 GENOMICS 77 (1-2): 105-113 Nurmi EL; Bradford Y; Chen YH; Hall J; Arnone B; et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families | 21 | 32 |
| 4480 | 4 | 28 | 7953 2002 GENOMICS 79 (6): 793-798 Premstaller A; Oberacher H; Rickert A; Huber CG; Oefner PJ Multiplex analysis of single-nucleotide extension products on a 16-capillary, denaturing, high-performance liquid chromatography array | 6 | 11 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4481 | 8 | 20 | 7954 2002 GENOMICS 80 (2): 129-134 Sultana R; Yu CE; Yu J; Munson J; Chen DH; et al. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins | 5 | 9 |
| 4482 | 4 | 50 | 7955 2002 GENOMICS 80 (2): 185-194 Yamagata T; Aradhya S; Mori M; Inoue K; Momoi MY; et al. The human secretin gene: Fine structure in 11p15.5 and sequence variation in patients with autism | 0 | 3 |
| 4483 | 6 | 30 | 7956 2002 GENOMICS 80 (3): 283-294 Vincent JB; Petek E; Thevarkunnel S; Kolozsvari D; Cheung J; et al. The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system | 1 | 7 |
| 4484 | 3 | 25 | 7957 2002 GENOMICS 80 (6): 585-592 Robledo R; Orru S; Sidoti A; Muresu R; Esposito D; et al. A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin | 0 | 7 |
| 4485 | 11 | 50 | 8523 2003 GENOMICS 81 (2): 166-174 Fletcher B; Goldstein DB; Bradman ALR; Weale ME; Bradman N; et al. High-throughput analysis of informative CYP2D6 compound haplotypes | 0 | 0 |
| 4486 | 10 | 22 | 9073 2004 GENOMICS 83 (6): 1046-1052 Repping S; van Daalen SKM; Korver CM; Brown LG; Marszalek JD; et al. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region | 3 | 6 |
| 4487 | 3 | 50 | 9542 2005 GENOMICS 85 (3): 352-359 Cui ZQ; Zharikov S; Xia SL; Anderson SI; Law AS; et al. Molecular cloning, characterization, and chromosomal assignment of porcine cationic amino acid transporter-1 | 0 | 0 |
| 4488 | 6 | 46 | 9543 2005 GENOMICS 85 (5): 563-573 Coussens AK; van Daal A Linkage disequilibrium analysis identifies an FGFR1 haplotype-tag SNP associated with normal variation in craniofacial shape | 0 | 0 |
| 4489 | 4 | 28 | 1124 1979 GENUS 35 (3-4): 23-39 CONTERIO F POPULATION-GENETICS AND DEMOGRAPHY | 0 | 0 |
| 4490 | 3 | 9 | 1125 1979 GENUS 35 (3-4): 41-50 BARRAI I GENETIC DRIFT, GENETIC DISTANCES AND GEOGRAPHIC DISTANCES | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 4491 | 1 | 16 | 601 1973 GEOGRAPHICAL ANALYSIS 5 (3): 245-261 MONMONIE.MS MAXIMUM-DIFFERENCE BARRIERS - ALTERNATIVE NUMERICAL REGIONALIZATION METHOD | 0 | 3 |
| 4492 | 3 | 17 | 827 1976 GEOGRAPHICAL ANALYSIS 8 (2): 215-223 CRUMPACKER DW; ZEI G; MORONI A; CAVALLISFORZA LL AIR DISTANCE VERSUS ROAD DISTANCE AS A GEOGRAPHICAL MEASURE FOR STUDIES ON HUMAN POPULATION-STRUCTURE | 14 | 14 |
| 4493 | 3 | 22 | 1944 1985 GEOGRAPHICAL ANALYSIS 17 (4): 263-283 WARTENBERG D MULTIVARIATE SPATIAL CORRELATION - A METHOD FOR EXPLORATORY GEOGRAPHICAL ANALYSIS | 5 | 26 |
| 4494 | 5 | 112 | 7958 2002 GEOGRAPHICAL REVIEW 92 (4): 526-544 Harris DR "The farther reaches of human time": Retrospect on Carl Sauer as prehistorian | 0 | 0 |
| 4495 | 2 | 5 | 6023 1998 GERONTOLOGY 44 (6): 349-349 Ivanova R; Lepage V; Charron D; Schachter F Mitochondrial genotype associated with French Caucasian centenarians | 2 | 27 |
| 4496 | 2 | 26 | 219 1964 GIORNALE DI MICROBIOLOGIA 12 (1-2): 15-& PETRINI M; GRASSI L; CAVA L RICERCHE IN VITRO SULLINTERAZIONE DELLA DEMETILCLORTETRACICLINA CON LERITROMICINA | 0 | 1 |
| 4497 | 7 | 20 | 682 1974 GIORNALE DI MICROBIOLOGIA 22 (1-2): 77-84 DETTORI R; NERI MG; ZAMPIERI A ECOLOGY OF SEX-SPECIFIC BACTERIOPHAGES | 0 | 0 |
| 4498 | 2 | 14 | 7959 2002 GIORNALE DI NEUROPSICOFARMACOLOGIA 24 (1): 5-12 Gigli GL Narcolepsy: A treatable, but underdiagnosed condition, although disabling and potentially dangersous - Part II | 0 | 0 |
| 4499 | 3 | 196 | 8524 2003 GLOBAL NETWORKS-A JOURNAL OF TRANSNATIONAL AFFAIRS 3 (3): 315-336 Sanjek R Rethinking migration, ancient to future | 0 | 1 |
| 4500 | 2 | 43 | 3796 1992 GLYCOCONJUGATE JOURNAL 9 (1): 56-62 DICIOCCIO RA; MILLER AL BINDING-RECEPTORS FOR ALPHA-L-FUCOSIDASE IN HUMAN B-LYMPHOID CELL-LINES | 0 | 3 |
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