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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 24: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2301 | 13 | 18 | 981 1992 HUMAN GENETICS 89(1):114-116 WOHRLE D; HIRST MC; KENNERKNECHT I; DAVIES KE; STEINBACH P GENOTYPE MOSAICISM IN FRAGILE-X FETAL TISSUES | 32 | 43 |
| 2302 | 18 | 23 | 903 1992 AMERICAN JOURNAL OF HUMAN GENETICS 51(2):299-306 WOHRLE D; KOTZOT D; HIRST MC; MANCA A; KORN B; SCHMIDT A; BARBI G; ROTT HD; POUSTKA A; DAVIES KE; STEINBACH P A MICRODELETION OF LESS THAN 250 KB, INCLUDING THE PROXIMAL PART OF THE FMR-I GENE AND THE FRAGILE-X SITE, IN A MALE WITH THE CLINICAL PHENOTYPE OF FRAGILE-X SYNDROME | 73 | 121 |
| 2303 | 27 | 51 | 1685 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; Schindler D; Vogel W; Steinbach P Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 15 | 28 |
| 2304 | 18 | 34 | 1967 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 7 |
| 2305 | 5 | 21 | 1422 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 9 | 18 |
| 2306 | 9 | 24 | 862 1991 HUMAN GENETICS 87(4):421-424 WOHRLE D; STEINBACH P FRAGILE-X EXPRESSION AND X-INACTIVATION .2. THE FRAGILE SITE AT XQ27.3 HAS A BASIC FUNCTION IN THE PATHOGENESIS OF FRAGILE X-LINKED MENTAL-RETARDATION | 6 | 8 |
| 2307 | 10 | 36 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):213-225 WOLFF PH; GARDNER J; LAPPEN J; PACCIA J; MERYASH D VARIABLE EXPRESSION OF THE FRAGILE-X SYNDROME IN HETEROZYGOUS FEMALES OF NORMAL INTELLIGENCE | 28 | 35 |
| 2308 | 11 | 24 | 623 1989 AMERICAN JOURNAL ON MENTAL RETARDATION 93(4):406-411 WOLFF PH; GARDNER J; PACCIA J; LAPPEN J THE GREETING BEHAVIOR OF FRAGILE X-MALES | 25 | 38 |
| 2309 | 1 | 26 | 237 1985 AMERICAN JOURNAL OF DANCE THERAPY 8:67-80 WOLFSCHEIN EG; FISCH GS; COHEN IL A STUDY OF THE USE OF NONVERBAL SYSTEMS IN THE DIFFERENTIAL-DIAGNOSIS OF AUTISTIC, MENTALLY-RETARDED AND FRAGILE X-INDIVIDUALS | 0 | 0 |
| 2310 | 0 | 1 | 596 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):457-458 WOLFSCHEIN EG; JENKINS EC; SKLOWER S; COHEN IL; WISNIEWSKI KE; BROWN WT ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2311 | 18 | 33 | 1010 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| 2312 | 11 | 36 | 399 1986 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 25(5):641-644 WRIGHT HH; YOUNG SR; EDWARDS JG; ABRAMSON RK; DUNCAN J FRAGILE X-SYNDROME IN A POPULATION OF AUTISTIC-CHILDREN | 16 | 21 |
| 2313 | 0 | 0 | 1269 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):585-585 WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY D; TAYLOR A; HAGERMAN RJ A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2314 | 22 | 31 | 1435 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):350-355 WrightTalamante C; Cheema A; Riddle JE; Luckey DW; Taylor AK; Hagerman RJ A controlled study of longitudinal IQ changes in females and males with fragile X syndrome | 11 | 13 |
| 2315 | 0 | 0 | 1716 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A403-A403 Xu B; School JM; Buroker NE; Scott CR; Chen SH High frequency of the FMR-1 INV10+14c/t polymorphism in Asians, and its association with the Fragile X Syndrome in Caucasians. | 0 | 1 |
| 2316 | 1 | 6 | 190 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 2317 | 16 | 47 | 2324 2004 CURRENT BIOLOGY 14(12):1025-1034 Xu KY; Bogert BA; Li WJ; Su K; Lee A; Gao FB The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1 | 0 | 0 |
| 2318 | 16 | 20 | 1082 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; NIIKAWA N; MASUNO I; KAJII T; HORI T PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 2319 | 6 | 10 | 986 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):195-203 YAMAUCHI M; SEKI N; HORI TA RAPID PREPARATION OF DIAGNOSTIC PROBES FOR THE FRAGILE-X SYNDROME BY DIRECT PCR AMPLIFICATION OF HUMAN CHROMOSOMAL DNA | 4 | 7 |
| 2320 | 0 | 0 | 1055 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1765-1765 YANAMANDRA K; RAO N; PETTENATI MJ; THOMAS IT UNEXPLAINED FRAGILE X-SYNDROME DNA TEST-RESULTS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2321 | 0 | 0 | 1549 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A389-A389 Ye LL; Ju W; Xu WM; Schupf N; Jenkins EC; Brown WT; Zhong N Distribution of apolipoprotein E genotypes in the fragile X syndrome, Batten disease, and Down syndrome populations. | 0 | 0 |
| 2322 | 17 | 30 | 2108 2002 ARQUIVOS DE NEURO-PSIQUIATRIA 60(4):981-985 Yonamine SM; da Silva AA Characteristics of the communication in individuals with fragile X syndrome | 0 | 0 |
| 2323 | 19 | 34 | 1801 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 2324 | 6 | 7 | 1126 1993 LANCET 342(8878):1004-1005 YOUNG ID DIAGNOSING FRAGILE-X SYNDROME | 1 | 1 |
| 2325 | 12 | 26 | 409 1986 SOUTHERN MEDICAL JOURNAL 79(4):405-409 YOUNG RS; JARAMILLO C; MCCOMBS JL; MOORE CM; JORGENSON RJ FRAGILE-X MENTAL-RETARDATION SYNDROME TRANSMITTED THROUGH INTELLECTUALLY NORMAL MALES - IMPLICATIONS FOR GENETIC-COUNSELING | 3 | 6 |
| 2326 | 0 | 0 | 745 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 YU S; KREMER E; PRITCHARD M; LYNCH M; NANCARROW J; BAKER E; HOLMAN K; MULLEY JC; WARREN ST; SCHLESSINGER D; RICHARDS RI; SUTHERLAND GR THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 2327 | 15 | 30 | 901 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):968-980 YU S; MULLEY J; LOESCH D; TURNER G; DONNELLY A; GEDEON A; HILLEN D; KREMER E; LYNCH M; PRITCHARD M; SUTHERLAND GR; RICHARDS RI FRAGILE-X SYNDROME - UNIQUE GENETICS OF THE HERITABLE UNSTABLE ELEMENT | 93 | 174 |
| 2328 | 3 | 9 | 898 1991 SCIENCE 252(5009):1179-1181 YU S; PRITCHARD M; KREMER E; LYNCH M; NANCARROW J; BAKER E; HOLMAN K; MULLEY JC; WARREN ST; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 274 | 537 |
| 2329 | 1 | 1 | 723 1990 NUCLEIC ACIDS RESEARCH 18(3):690-690 YU S; SUTHERS GK; MULLEY JC A BCLI RFLP FOR DXS296 (VK21) NEAR THE FRAGILE-X | 2 | 6 |
| 2330 | 9 | 21 | 705 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 6 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2331 | 0 | 0 | 2087 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):377-377 Zabala WM; Nava N; Gonzalez S; Delgado W; Borjas L; Fernandez E; Rojas A; Pineda L Clinical and molecular analysis of the fragile X syndrome in mentally retarded males from the Venezuelan northwestern region. | 0 | 0 |
| 2332 | 2 | 6 | 369 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| 2333 | 34 | 62 | 2253 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; Reis S; Oostra B; Bagni C The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses | 16 | 38 |
| 2334 | 0 | 0 | 2133 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Zalfa F; Primerano B; Lauro C; Giorgi M; Moro A; Spinelli G; Tongiorgi E; Costra B; Amaldi F; Bagni C Towards an understanding of the Fragile X syndrome: FMRP is translated at the synapses where it acts as a translational regulator | 0 | 0 |
| 2335 | 0 | 5 | 59 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 2336 | 0 | 0 | 762 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):280-280 ZASLAV AL; BROWN WT THE SIGNIFICANCE OF LOW-LEVEL FRAGILE X EXPRESSION | 0 | 0 |
| 2337 | 0 | 0 | 1451 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G4-G4 Zehnbauer BA Fragile X molecular detection in clinical referrals. | 0 | 0 |
| 2338 | 16 | 36 | 1347 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; NUSSBAUM RL; DREYFUSS G THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 63 | 111 |
| 2339 | 18 | 37 | 2007 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; Speese SD; Rubin GM; Broadie K Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 36 | 71 |
| 2340 | 18 | 58 | 2325 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307 Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; Friedman D; Broadie K The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2341 | 0 | 0 | 2354 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; Tan E Fragile X premutation alleles in patients with sporadic cerebellar ataxia | 0 | 0 |
| 2342 | 1 | 8 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; MA SW; LO WHY; WU GY; CHENG ZY; ZHANG XZ FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 0 | 1 |
| 2343 | 0 | 0 | 1040 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):744-744 ZHONG N; DOBKIN C; BROWN WT A 2ND HYPERMUTABLE DNA-SEQUENCE LOCATED WITHIN THE FRAGILE X-GENE | 0 | 0 |
| 2344 | 7 | 31 | 1139 1993 NATURE GENETICS 5(3):248-253 ZHONG N; DOBKIN C; BROWN WT A COMPLEX MUTABLE POLYMORPHISM LOCATED WITHIN THE FRAGILE X-GENE | 29 | 58 |
| 2345 | 14 | 23 | 1755 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):268-271 Zhong N; Ju W; Nelson D; Dobkin C; Brown WT Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation | 3 | 5 |
| 2346 | 0 | 0 | 1547 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A324-A324 Zhong N; Ju W; Xu WM; Liu B; Dobkin C; Brown WT Molecular pathogenetic studies of the fragile X syndrome: A candidate transcript targeted by the fragile X protein FMRP. | 0 | 0 |
| 2347 | 3 | 13 | 1759 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):309-310 Zhong N; Ju WN; Brown WT; Ye LL; Jenkins EC; Schupf N Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease | 0 | 0 |
| 2348 | 19 | 28 | 1421 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; Brown WT Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 26 |
| 2349 | 20 | 34 | 1745 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; Wu GY; Chen SH; Jin RM; Hu XF; Yang AD; Liu XX; Poon P; Pang C; Zheng Y; Song L; Zhao P; Fu BJ; Gu HJ; Brown WT Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 6 | 10 |
| 2350 | 28 | 43 | 1416 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang DW; Ju MN; Nolin S; Dobkin C; Ryynanen M; Brown WT Fragile X founder effects and new mutations in Finland | 9 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2351 | 19 | 51 | 1261 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(2):351-361 ZHONG N; YANG WH; DOBKIN C; BROWN WT FRAGILE-X GENE INSTABILITY - ANCHORING AGGS AND LINKED MICROSATELLITES | 38 | 79 |
| 2352 | 11 | 25 | 1172 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):405-411 ZHONG N; YE LL; DOBKIN C; BROWN WT FRAGILE-X FOUNDER CHROMOSOME EFFECTS - LINKAGE DISEQUILIBRIUM OR MICROSATELLITE HETEROGENEITY | 17 | 29 |
| 2353 | 0 | 0 | 1975 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):438-438 Zhou Y; Chong SS Simplified molecular diagnostic testing for fragile X syndrome using methylation-specific PCR (ms-PCR). | 0 | 0 |
| 2354 | 10 | 16 | 2339 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; Ng ISL; Chong SS Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| 2355 | 1 | 2 | 276 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):788-788 ZOLL B; ARNEMANN J; KRAWCZAK M; COOPER DN; PESCIA G; WAHLI W; STEINBACH P; SCHMIDTKE J THE LOCI FOR FRAGILE X-MENTAL RETARDATION SYNDROME AND COAGULATION FACTOR-IX ARE NOT CLOSELY LINKED | 0 | 0 |
| 2356 | 5 | 52 | 161 1983 SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT 113(7):238-244 ZOLLINGER A; SCHMID W; VILAN J; SORG B; KNOBLAUCH M X-LINKED MENTAL-RETARDATION WITH FRAGILE X-CHROMOSOME AND MACROORCHIDISM | 3 | 3 |
| 2357 | 1 | 7 | 29 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| 2358 | 0 | 0 | 199 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 2359 | 5 | 12 | 400 1986 LANCET 2(8517):1191-1192 [Anon] PREVENTIVE SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2360 | 1 | 2 | 449 1987 HASTINGS CENTER REPORT 17(1):2-3 [Anon] TO SCREEN OR NOT TO SCREEN FOR THE FRAGILE X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2361 | 1 | 1 | 963 1992 ARCHIVES OF DISEASE IN CHILDHOOD 67(11):1337-1337 [Anon] SISTERS OF FRAGILE-X BOYS | 0 | 0 |
| 2362 | 0 | 0 | 1193 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):606-614 [Anon] ABSTRACTS FOR THE 6TH INTERNATIONAL WORKSHOP ON FRAGILE-X-SYNDROME AND X-LINKED MENTAL-RETARDATION | 0 | 0 |
| 2363 | 0 | 0 | 1344 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):411-416 [Anon] 4th International Fragile X and X-Linked Mental Retardation Conference - Albuquerque, NM, USA, June 8-12, 1994 - Abstracts | 0 | 0 |
| 2364 | 2 | 4 | 1486 1996 INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS 52(2):209-210 [Anon] Fragile X syndrome | 0 | 0 |
| 2365 | 0 | 0 | 1887 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 2366 | 0 | 1 | 2013 2001 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 43(2):142-142 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) | 0 | 0 |
| 2367 | 0 | 0 | 2072 2001 REVISTA DE NEUROLOGIA 33:S88-S90 [Anon] Interdisciplinary conference on the fragile X syndrome - Barcelona, October 27-28, 2001 - Abstracts | 0 | 0 |
| 2368 | 0 | 0 | 2141 2002 GENETIC COUNSELING 13(2):207-261 [Anon] Abstracts of the 10th International Workshop on Fragile X and X-Linked Mental Retardation - 19-22 September 2001, Frascati, Italy | 0 | 0 |
| 2369 | 0 | 0 | 2328 2004 GENETIC COUNSELING 15(2):239-286 [Anon] Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus | 0 | 0 |
Page 24: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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Version: 2004.08.24