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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 15: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1401 | 0 | 0 | 1401 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):6-6 Maes B; Borghraef M; Fryns JP Presentation of a fragile-X screening list. | 0 | 0 |
| 1402 | 0 | 0 | 1402 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):14-14 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mandel JL; Mattei JF A rare example of a reverse mutation in a fragile X syndrome family. | 0 | 0 |
| 1403 | 0 | 0 | 1403 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):16-16 Murray A; Conway GS; Jacobs PA Premature ovarian failure and fragile X. | 0 | 0 |
| 1404 | 0 | 0 | 1404 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):17-17 Oostra BA; Willemsen R; Mandel JL; DeVries B; Devys D Rapid screening test for fragile X syndrome. | 0 | 0 |
| 1405 | 0 | 0 | 1405 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):19-19 Shen Y; Zhu N; Huang D; Wu GY Studies on fragile X syndrome in the Chinese. | 0 | 0 |
| 1406 | 0 | 0 | 1406 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):25-25 deVries BBA; vandenOuweland AMW; Mohkamsing S; Halley DJJ; Tibben A; Oostra BA; Galjaard H; Niermeijer MF Acceptance of screening for the fragile X syndrome among 1878 mentally retarded individuals in institutions and special schools in the Netherlands | 0 | 0 |
| 1407 | 4 | 21 | 1407 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 | 1 | 30 |
| 1408 | 11 | 12 | 1408 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 5 | 6 |
| 1409 | 10 | 12 | 1409 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; MenapaceDrew G; Bick DP; Levinson G; Schulman JD; HowardPeebles PN Molecular fragile X screening in normal populations | 13 | 17 |
| 1410 | 9 | 10 | 1410 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; Lituania M; Buscaglia M; Giussani U; Grimoldi MG; Bricarelli FD Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 16 | 24 | 1411 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; Li SY; StarkHouck S; Brophy P; Duncan C; Dobkin C; Jenkins E Prenatal diagnosis and carrier screening for fragile X by PCR | 16 | 25 |
| 1412 | 11 | 12 | 1412 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):196-197 Turner G; Webb T; Wake S; Robinson H Prevalence of fragile X syndrome | 137 | 223 |
| 1413 | 4 | 11 | 1413 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 1414 | 30 | 50 | 1414 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 9 | 23 |
| 1415 | 24 | 59 | 1415 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; DagnaBricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 11 | 24 |
| 1416 | 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 |
| 1417 | 13 | 20 | 1417 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 5 | 15 |
| 1418 | 10 | 20 | 1418 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):241-245 Kooy RF; DHooge R; Reyniers E; Bakker CE; Nagels G; DeBoulle K; Storm K; Clincke G; DeDeyn PP; Oostra BA; Willems PJ Transgenic mouse model for the fragile X syndrome | 22 | 41 |
| 1419 | 13 | 37 | 1419 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; Bakker CE; Oostra BA; Kooy RF; Willems PJ Long-term potentiation in the hippocampus of fragile X knockout mice | 22 | 31 |
| 1420 | 17 | 21 | 1420 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 12 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 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 |
| 1422 | 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 |
| 1423 | 7 | 13 | 1423 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| 1424 | 12 | 21 | 1424 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; Warren ST; Tarleton J A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| 1425 | 21 | 35 | 1425 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Reverse mutations in the fragile X syndrome | 9 | 18 |
| 1426 | 16 | 20 | 1426 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 8 | 9 |
| 1427 | 17 | 24 | 1427 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; Ding XH; Jenkins EC; Zhong N; Brown WT Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| 1428 | 29 | 43 | 1428 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; Oostra BA; vandenOuweland AMW The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 11 | 13 |
| 1429 | 18 | 21 | 1429 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 12 | 15 |
| 1430 | 4 | 9 | 1430 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; Holden JJA Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 12 | 31 | 1431 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 5 | 7 |
| 1432 | 14 | 24 | 1432 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; Humphries T; Ray PN; Teshima IE Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| 1433 | 12 | 18 | 1433 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):334-339 Franke P; Maier W; Hautzinger M; Weiffenbach O; Gansicke M; Iwers B; Poustka F; Schwab SG; Froster U Fragile-X carrier females: Evidence for a distinct psychopathological phenotype? | 19 | 28 |
| 1434 | 18 | 29 | 1434 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):340-345 Sobesky WE; Taylor AK; Pennington BF; Bennetto L; Porter D; Riddle J; Hagerman RJ Molecular/clinical correlations in females with fragile X | 26 | 35 |
| 1435 | 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 |
| 1436 | 15 | 41 | 1436 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):356-361 Fisch GS; Simensen R; Tarleton J; Chalifoux M; Holden JJ; Carpenter N; HowardPeebles PN; Maddalena A Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis | 24 | 31 |
| 1437 | 10 | 14 | 1437 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; Tarleton J; JulienInalsingh C; Chalifoux M; Holden JJA Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| 1438 | 16 | 21 | 1438 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):365-369 Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; Brown WT Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males | 14 | 15 |
| 1439 | 3 | 7 | 1439 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 23 | 42 |
| 1440 | 2 | 2 | 1440 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 4 | 6 | 1441 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 1442 | 0 | 7 | 1442 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):378-381 Wingrove EJ; Norris J; Barton PL; Hagerman R Experiences and attitudes concerning genetic testing and insurance in a Colorado population: A survey of families diagnosed with fragile X syndrome | 0 | 8 |
| 1443 | 3 | 18 | 1443 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 1444 | 14 | 19 | 1444 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| 1445 | 12 | 20 | 1445 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):413-414 Loesch DZ Fragile X: Clinical associations | 0 | 0 |
| 1446 | 15 | 25 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; Sherman SL Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 9 | 25 |
| 1447 | 1 | 1 | 1447 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(3):527-527 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus (vol 64, pg 234, 1996) | 0 | 0 |
| 1448 | 0 | 3 | 1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 65(4):355-356 Seemanova E Fragile X syndrome in incestuous families | 0 | 0 |
| 1449 | 1 | 1 | 1449 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 66(1):118-118 Perroni L; Grasso M; Argusti A; Nigro CL; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families (vol 64, pg 176, 1996) | 0 | 0 |
| 1450 | 11 | 28 | 1450 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 0 | 0 | 1451 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G4-G4 Zehnbauer BA Fragile X molecular detection in clinical referrals. | 0 | 0 |
| 1452 | 0 | 0 | 1452 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G5-G5 Larsen LA; NorgaardPedersen B; Vuust J Analysis of fragile X CGG repeats in the normal range by PCR amplification and automated capillary electrophoresis. | 0 | 0 |
| 1453 | 0 | 0 | 1453 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G6-G6 Pandya A; FerreiraGonzalez A; JacksonCook C; Ware JL; Garrett CT Evaluation of fragile X CCG locus using PCR and a fluorescent automated DNA sequencer. | 0 | 0 |
| 1454 | 10 | 25 | 1454 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328 Mark HFL; Bier JAB; Scola P The frequency of chromosomal abnormalities in patients referred for fragile X analysis | 1 | 4 |
| 1455 | 19 | 37 | 1455 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 1456 | 1 | 1 | 1456 1996 ARCHIVES OF DISEASE IN CHILDHOOD 74(1):88-88 Magnay D; Morritt J; Waterston T Fragile X syndrome | 0 | 0 |
| 1457 | 0 | 1 | 1457 1996 ARCHIVES OF MEDICAL RESEARCH 27(3):427-427 DiazGallardo Molecular characterization of the fragile-x syndrome in the Mexican population (vol 26, pg S77, 1995) | 0 | 0 |
| 1458 | 4 | 13 | 1458 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1459 | 11 | 81 | 1459 1996 BIOCHEMISTRY 35(15):5041-5053 Pearson CE; Sinden RR Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | 3 | 84 |
| 1460 | 0 | 0 | 1460 1996 BIOLOGICALS 24(3):210-210 Chehab FF; Wall J; Cai SP Lessons derived from the clinical molecular diagnosis of cystic fibrosis, thalassaemia, Fragile X and Huntington's disease | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 0 | 0 | 1461 1996 BIOPHYSICAL JOURNAL 70(2):SU496-SU496 Chen X; Mariappan SVS; Ratliff R; Moyzis RK; Smith SS; Bradbury EM; Gupta G The formation and methylation of the ''slippage structures'' in vitro: The molecular basis of the fragile-X syndrome | 0 | 0 |
| 1462 | 0 | 1 | 1462 1996 BRITISH JOURNAL OF DEVELOPMENTAL PSYCHOLOGY 14:247-248 Happe F Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1463 | 9 | 43 | 1463 1996 CELL 85(2):237-245 Musco G; Stier G; Joseph C; Morelli MAC; Nilges M; Gibson TJ; Pastore A Three-dimensional structure and stability of the KH domain: Molecular insights into the fragile X syndrome | 20 | 167 |
| 1464 | 64 | 95 | 1464 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 8 |
| 1465 | 0 | 3 | 1465 1996 CHINESE SCIENCE BULLETIN 41(5):436-437 Huang T; Shen Y; Fan Y; Wu GY Expression of two alternative splicing isoforms of fragile X gene in human placenta | 0 | 0 |
| 1466 | 0 | 0 | 1466 1996 CLINICAL CHEMISTRY 42(6):441-441 Tsongalis GJ; Hodges KA; Adkins S; Silverman LM Chemiluminescent detection of the CGG trinucleotide repeat expansion in fragile X syndrome. | 0 | 0 |
| 1467 | 0 | 0 | 1467 1996 CLINICAL CHEMISTRY 42(11):7-7 Hamdan H; Bailey A; Martinez JJ; Fenwick R; Leon JA Improved amplification and automated detection of trinucleotide repeats in the diagnosis of fragile X syndrome. | 0 | 0 |
| 1468 | 11 | 21 | 1468 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782 Finucane B Should all pregnant women be offered carrier testing for fragile X syndrome? | 1 | 1 |
| 1469 | 37 | 74 | 1469 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 6 | 8 |
| 1470 | 13 | 56 | 1470 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; Wan L; Dreyfuss G Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene | 2 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 0 | 1 | 1471 1996 CONTEMPORARY PSYCHOLOGY 41(5):488-489 McGraw KO Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1472 | 60 | 94 | 1472 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
| 1473 | 15 | 39 | 1473 1996 EMBO JOURNAL 15(19):5408-5414 Fridell RA; Benson RE; Hua J; Bogerd HP; Cullen BR A nuclear role for the fragile X mental retardation protein | 32 | 65 |
| 1474 | 19 | 27 | 1474 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mattei JF Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 4 | 6 |
| 1475 | 21 | 44 | 1475 1996 EUROPEAN PSYCHIATRY 11(5):227-232 Barbe B; Franke P; Maier W; Leboyer M Fragile X syndrome .1. An overview on its genetic mechanism | 0 | 0 |
| 1476 | 58 | 71 | 1476 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 4 | 5 |
| 1477 | 0 | 0 | 1477 1996 FASEB JOURNAL 10(6):D30-D30 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. | 0 | 0 |
| 1478 | 0 | 4 | 1478 1996 GENETIC COUNSELING 7(3):227-230 Fryns JP; DHooghe M; Devriendt K Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene | 0 | 0 |
| 1479 | 7 | 14 | 1479 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 1480 | 40 | 62 | 1480 1996 GIORNALE DI NEUROPSICHIATRIA DELL ETA EVOLUTIVA 16(2):147-154 Veneselli E; Biancheri R; Perrone MV Neuropsychiatric aspects in the fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 17 | 26 | 1481 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 4 | 8 |
| 1482 | 15 | 26 | 1482 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 7 | 16 |
| 1483 | 5 | 55 | 1483 1996 HUMAN GENETICS 98(2):151-157 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines | 2 | 26 |
| 1484 | 29 | 49 | 1484 1996 HUMAN MOLECULAR GENETICS 5(3):319-330 Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome | 22 | 46 |
| 1485 | 17 | 53 | 1485 1996 HUMAN MOLECULAR GENETICS 5(8):1083-1091 Eberhart DE; Malter HE; Feng Y; Warren ST The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals | 74 | 120 |
| 1486 | 2 | 4 | 1486 1996 INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS 52(2):209-210 [Anon] Fragile X syndrome | 0 | 0 |
| 1487 | 6 | 29 | 1487 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; Lachiewicz A; Reiss A; Freund L; Hagerman R; OConnor R Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 17 | 21 |
| 1488 | 5 | 37 | 1488 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 1 | 22 |
| 1489 | 11 | 50 | 1489 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 2 | 38 |
| 1490 | 0 | 0 | 1490 1996 JOURNAL OF INVESTIGATIVE MEDICINE 44(1):A119-A119 Merenstein SA; Sobesky WE; Taylor AK; Tran HX; Riddle JE; Hagerman RJ Molecular clinical correlations in males with fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 10 | 13 | 1491 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; Estivill X Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 9 | 15 |
| 1492 | 15 | 21 | 1492 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 1493 | 13 | 20 | 1493 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; vanHemel JO; vandenOuweland AMW; Niermeijer MF; Oostra BA; Halley DJJ Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| 1494 | 0 | 0 | 1494 1996 JOURNAL OF NEUROCHEMISTRY 67:S34-S34 Chen TA; Lu XF; Yi YH; Ho WKK Analysis of a CGG sequence at the FMR-1 locus in fragile X site by PCR-DGGE method. | 0 | 0 |
| 1495 | 0 | 0 | 1495 1996 JOURNAL OF NEUROCHEMISTRY 67:S36-S36 Chen TA; Lu XF; Ilo WKK; Yi YH; Chen SQ; Chen Z Variation of the CGG repeat in FMR-1 gene in non retarded Chinese population and fragile X syndrome patients | 0 | 0 |
| 1496 | 12 | 14 | 1496 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 10 | 20 |
| 1497 | 1 | 4 | 1497 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; Stefanini MC Normal respiratory pattern during sleep in young fragile X-syndrome patients | 1 | 1 |
| 1498 | 9 | 33 | 1498 1996 KOREAN JOURNAL OF GENETICS 18(3):199-210 Choi SK; Kim HY; Paik YK Cytogenetic analysis of a Korean family with fragile X syndrome | 0 | 1 |
| 1499 | 3 | 4 | 1499 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 1500 | 3 | 45 | 1500 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
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