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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1901 | 0 | 0 | 1289 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1941-1941 TSAI MS; CHIEN TY; YANG YL; CHEN HR; HWANG SM IDENTIFICATION OF THE NUMBER OF THE FRAGILE-X SYNDROME CGG REPEAT USING SILVER STAIN | 0 | 0 |
| 1902 | 1 | 9 | 1298 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 1903 | 0 | 0 | 1303 1995 ANNALS OF NEUROLOGY 38(3):499-499 BERRYKRAVIS E; CIURLIONIS R OVEREXPRESSION OF FRAGILE-X GENE (FMR-1) TRANSCRIPTS IN NEURAL CELLS RESULTS IN INCREASED LEVELS OF CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION | 0 | 0 |
| 1904 | 2 | 5 | 1307 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(6):544-544 TURK J TREATMENT OF FRAGILE-X SYNDROME | 0 | 0 |
| 1905 | 0 | 0 | 1310 1995 BIOLOGICAL PSYCHIATRY 37(9):629-629 REISS AL FRAGILE-X SYNDROME | 0 | 0 |
| 1906 | 2 | 6 | 1311 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; DURRANT S ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1907 | 4 | 5 | 1313 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1908 | 4 | 7 | 1314 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| 1909 | 0 | 0 | 1315 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1910 | 0 | 0 | 1316 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 0 | 1 | 1317 1995 BRITISH JOURNAL OF PSYCHIATRY 166:688-688 COOKE LB BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,E | 0 | 0 |
| 1912 | 0 | 0 | 1319 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1913 | 0 | 0 | 1321 1995 CYTOGENETICS AND CELL GENETICS 69(1-2):116-116 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST | 0 | 0 |
| 1914 | 9 | 23 | 1322 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):167-184 Hagerman R; Staley L; Brown WT; Taylor A; Meadow K; Dorn M; Stoorman S; Neri G; Chiurazzi P; Levitas A; Spiridigliozzi GA; OConnor R; Weber JD; Braden M; Sudhalter V Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation | 0 | 0 |
| 1915 | 0 | 0 | 1323 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):185-186 Nommensen D Report of the Executive Director of the National Fragile X Foundation | 0 | 0 |
| 1916 | 11 | 21 | 1334 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):319-326 Wake SA; Robinson H Assessment of counselling of normal males and normal transmitting male carriers identified in fragile X families | 0 | 0 |
| 1917 | 2 | 23 | 1337 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):345-352 Rattazzi MC Protein therapy in fragile X syndrome - A brief overview of principles, potentials and problems | 0 | 0 |
| 1918 | 0 | 7 | 1338 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1919 | 0 | 0 | 1339 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):363-366 Glass L Females with fragile X: A parent's perspective | 0 | 0 |
| 1920 | 5 | 9 | 1340 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):370-379 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 7 | 18 | 1342 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; Dykens E Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1922 | 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 |
| 1923 | 13 | 16 | 1345 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1924 | 0 | 0 | 1348 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1925 | 0 | 0 | 1349 1995 EPILEPSIA 36:S244-S244 SINGH R; SUTHERLAND G; MANSON J SEIZURES WITH EPILEPTOGENIC EEG PATTERN IN 2 SISTERS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1926 | 0 | 0 | 1350 1995 FASEB JOURNAL 9(6):A1324-A1324 SMITH SS; LAAYOUN A; BAKER DJ; KHO MR RECOGNITION OF TELOMERE-LIKE STRUCTURES FROM THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X BY HUMAN DNA METHYLTRANSFERASE | 0 | 0 |
| 1927 | 3 | 4 | 1351 1995 GENETIC COUNSELING 6(2):97-101 BORGHGRAEF M; SWILLEN A; VANDENBERGHE H; FRYNS JP FRAGILE-X BOYS - EVOLUTION OF THE MENTAL AGE IN CHILDHOOD - PRELIMINARY DATA ON 10 PREPUBERTAL BOYS | 0 | 0 |
| 1928 | 0 | 0 | 1362 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :373-373 WILLEMS PJ; BAKKER CE; REYNIERS E; VERHEIJ C; DEBOULLE K; OOSTRA BA A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1929 | 0 | 1 | 1363 1995 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 36(4):707-707 TURK J BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,EM, HODAPP,RM, LECKMAN,JF | 0 | 0 |
| 1930 | 0 | 0 | 1368 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 WANG Q; GREEN EP; BOBROW M; MATHEW CG SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 0 | 0 | 1369 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| 1932 | 0 | 0 | 1370 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 1933 | 35 | 59 | 1379 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 1934 | 0 | 0 | 1380 1995 MOLECULAR BIOLOGY OF THE CELL 6:1801-1801 TANEJA KL; NELSON D; SINGER RH SPATIAL-DISTRIBUTION OF CGG REPEAT SEQUENCES IN NUCLEI OF FRAGILE-X PATIENT CELLS | 0 | 0 |
| 1935 | 0 | 0 | 1383 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 1936 | 11 | 14 | 1384 1995 NEW ZEALAND MEDICAL JOURNAL 108(1009):404-406 NEVILLE L; COCHRANE J; FITZGERALD P; KENNEDY M FRAGILE-X MENTAL-RETARDATION SYNDROME - DNA DIAGNOSIS AND CARRIER DETECTION IN NEW-ZEALAND FAMILIES | 0 | 0 |
| 1937 | 15 | 19 | 1393 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJJ; Horst J; Mazurczak T Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| 1938 | 0 | 0 | 1399 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-1 Laing S; Robinson H; Wake S; Wright F; Turner G Normal males and their role in transmission of the fragile x syndrome. | 0 | 0 |
| 1939 | 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 |
| 1940 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 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 |
| 1942 | 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 |
| 1943 | 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 |
| 1944 | 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 |
| 1945 | 12 | 20 | 1445 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):413-414 Loesch DZ Fragile X: Clinical associations | 0 | 0 |
| 1946 | 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 |
| 1947 | 0 | 3 | 1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 65(4):355-356 Seemanova E Fragile X syndrome in incestuous families | 0 | 0 |
| 1948 | 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 |
| 1949 | 0 | 0 | 1451 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G4-G4 Zehnbauer BA Fragile X molecular detection in clinical referrals. | 0 | 0 |
| 1950 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 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 |
| 1952 | 1 | 1 | 1456 1996 ARCHIVES OF DISEASE IN CHILDHOOD 74(1):88-88 Magnay D; Morritt J; Waterston T Fragile X syndrome | 0 | 0 |
| 1953 | 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 |
| 1954 | 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 |
| 1955 | 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 |
| 1956 | 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 |
| 1957 | 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 |
| 1958 | 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 |
| 1959 | 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 |
| 1960 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 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 |
| 1962 | 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 |
| 1963 | 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 |
| 1964 | 7 | 14 | 1479 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 1965 | 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 |
| 1966 | 2 | 4 | 1486 1996 INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS 52(2):209-210 [Anon] Fragile X syndrome | 0 | 0 |
| 1967 | 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 |
| 1968 | 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 |
| 1969 | 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 |
| 1970 | 0 | 0 | 1507 1996 PEDIATRIC RESEARCH 39(2):371-371 Torrado M; Herrera J; Chertkoff L; Tenembaum S; Bin L; Barreiro C Diagnosis value of a pediatric clinical score for the diagnosis of the Fragile X Syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 23 | 49 | 1513 1996 REVISTA MEDICA DE CHILE 124(7):865-872 Jara L; Avendano I; Aspillaga M; Blanco R Molecular and genetic features of fragile X syndrome. A review | 0 | 0 |
| 1972 | 17 | 33 | 1516 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| 1973 | 5 | 20 | 1517 1996 VARIATION IN THE HUMAN GENOME 197:126-136 Weiss KM; Sutherland GR; Harper PS; Bodmer W; Bowcock AM; Freimer NB; Kidd KK; Chakraborty R; Armour J; Donnelly P; Clark A; Chakravarti A; Weatherall DJ; Edwards JH; Balmain A; Zechner R Unusual inheritance patterns due to dynamic mutation in fragile X syndrome - Discussion | 0 | 0 |
| 1974 | 0 | 1 | 1518 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):191-192 Fombonne E The fragile X syndrome | 0 | 0 |
| 1975 | 13 | 25 | 1519 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| 1976 | 13 | 24 | 1520 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):202-208 Hagerman RJ Fragile X syndrome: meeting the challenges of diagnosis and care | 0 | 0 |
| 1977 | 12 | 16 | 1521 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 1978 | 8 | 9 | 1522 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):221-223 Ponsot G Fragile X syndrome. Early recognition. | 0 | 0 |
| 1979 | 6 | 9 | 1523 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 1980 | 3 | 10 | 1524 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 13 | 27 | 1525 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):232-238 Turk J Treatments and services for individuals with fragile X syndrome and their families | 0 | 0 |
| 1982 | 0 | 0 | 1528 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; Maddalena A; Simensen R; Tarleton J; Borghgraef M; Steyaert J; Fryns JP Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 1983 | 0 | 0 | 1529 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| 1984 | 0 | 0 | 1530 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Corbin F; Bouillon M; Rousseau F; Khandjian EW The fragile-X mental retardation protein is a mRNA chaperone associated with translating complexes. | 0 | 0 |
| 1985 | 0 | 0 | 1531 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Brown VL; Small K; Lakkis L; Wilkinson KD; Warren ST Purification and characterization of the fragile X mental retardation protein. | 0 | 0 |
| 1986 | 0 | 0 | 1532 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| 1987 | 0 | 0 | 1533 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; Taylor AK A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 1988 | 0 | 0 | 1534 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A109-A109 Perroni L; Grasso M; Garavelli L; Argusti A; Cavani S; Lo Nigro C; Bricarelli FD Three cases of high functioning fragile X males | 0 | 0 |
| 1989 | 0 | 0 | 1535 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| 1990 | 0 | 0 | 1536 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 0 | 0 | 1537 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 1992 | 0 | 0 | 1538 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| 1993 | 0 | 0 | 1539 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 1994 | 0 | 0 | 1540 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| 1995 | 0 | 0 | 1541 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 1996 | 0 | 0 | 1542 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| 1997 | 0 | 0 | 1543 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A304-A304 Bat O; Kimmel M; Axelrod DE; Chakraborty R Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease. | 0 | 0 |
| 1998 | 0 | 0 | 1545 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; Ledbetter DH; Das S Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 1999 | 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 |
| 2000 | 0 | 0 | 1548 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Popovich B; Prior TW; Arinami T; Ravine D; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
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