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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 |
|---|---|---|---|---|---|
| 2101 | 21 | 41 | 1869 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 2102 | 11 | 14 | 1875 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| 2103 | 3 | 18 | 1878 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; Mandel JL; Shen Y Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 2104 | 0 | 0 | 1879 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 2105 | 6 | 13 | 1880 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| 2106 | 0 | 0 | 1885 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; Spangler CC; Greenough WT Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 2107 | 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 |
| 2108 | 11 | 12 | 1892 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 2109 | 0 | 0 | 1898 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 2110 | 0 | 0 | 1899 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; Oostra BA; Smits APT; Braat DDM Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2111 | 1 | 2 | 1901 2000 HUMAN REPRODUCTION 15(8):1874-1874 Rychlik DF Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 2112 | 1 | 2 | 1902 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 2113 | 0 | 0 | 1903 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| 2114 | 0 | 0 | 1907 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 2115 | 0 | 0 | 1908 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| 2116 | 0 | 0 | 1909 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 2117 | 0 | 0 | 1913 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; Karadottir S; Cawthon S Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 2118 | 0 | 0 | 1914 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Rabe A; Dumas R; Haubenstock H; Wen Y; Dobkin C; Jenkins E Progress fragile-X syndrome analysis | 0 | 0 |
| 2119 | 0 | 0 | 1915 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:247-247 Cornish KM; Munir F Profile of memory and attention problems in adults with fragile-X syndrome: Clinical and educational implications | 0 | 0 |
| 2120 | 0 | 0 | 1916 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2121 | 0 | 0 | 1917 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 2122 | 0 | 0 | 1919 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; Butler E; Loesch D; Hagerman RJ Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 2123 | 0 | 0 | 1920 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| 2124 | 0 | 0 | 1921 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; Chandra S; Bhaskaran GS; Brahmachari V Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 2125 | 0 | 0 | 1922 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| 2126 | 0 | 0 | 1923 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; Weissman M; Karadottir S; Cawthon S Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 2127 | 0 | 0 | 1924 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 2128 | 0 | 0 | 1925 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| 2129 | 0 | 0 | 1926 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 2130 | 0 | 0 | 1927 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2131 | 0 | 0 | 1928 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 2132 | 0 | 0 | 1929 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| 2133 | 0 | 0 | 1930 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; McKeown C; Davison EV An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 2134 | 0 | 0 | 1931 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 2135 | 0 | 0 | 1932 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| 2136 | 0 | 0 | 1933 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 2137 | 5 | 6 | 1937 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 2138 | 4 | 15 | 1938 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 0 | 0 |
| 2139 | 2 | 5 | 1939 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(2):264-266 Eliez S; Reiss AL Generics of childhood disorders: XI. Fragile X syndrome | 0 | 0 |
| 2140 | 1 | 5 | 1940 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2141 | 0 | 5 | 1941 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-399 Lombroso PJ Fragile X syndrome - Dr. Lombroso replies | 0 | 0 |
| 2142 | 11 | 17 | 1942 2000 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 99(5):402-407 Wang YC; Li C; Lin ML; Lin WH; Li SY Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese | 0 | 0 |
| 2143 | 0 | 1 | 1943 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 2144 | 27 | 53 | 1955 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 2145 | 32 | 54 | 1959 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; Treitman TM Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| 2146 | 7 | 10 | 1960 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 2147 | 1 | 5 | 1963 2000 REVISTA DE NEUROLOGIA 30(10):996-997 Serrano-Castro PJ; Serrano-Castillo P A historical description of the association of macro-orchidea, mental retardation and cranial dysmorphia in males (fragile X chromosome syndrome) by A.B Richerand | 0 | 0 |
| 2148 | 0 | 0 | 1965 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| 2149 | 0 | 0 | 1969 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 2150 | 0 | 0 | 1970 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2151 | 0 | 0 | 1971 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |
| 2152 | 0 | 0 | 1972 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 2153 | 0 | 0 | 1973 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; Belser R; Ding XH; Houck GE; Glicksman A; Dobkin CS; Nolin SL; Brown WT Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 2154 | 0 | 0 | 1974 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; Gawde HM Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 2155 | 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 |
| 2156 | 0 | 0 | 1976 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; Barcelo F; Rosell J A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 2157 | 0 | 0 | 1977 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| 2158 | 0 | 0 | 1978 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 2159 | 0 | 0 | 1979 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| 2160 | 0 | 0 | 1980 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; Li SH; Brooks S; Dobkin C; Jenkins EC The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2161 | 0 | 0 | 1981 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; Sanchez A; Mila M Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| 2162 | 4 | 7 | 1985 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 0 |
| 2163 | 0 | 0 | 1989 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| 2164 | 1 | 1 | 1990 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Moore CJ; Daly E; Tassone F; Jacobs PA; Davies KE; Murphy KC; Murphy KGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2165 | 0 | 0 | 1997 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 2166 | 15 | 30 | 1998 2001 ARQUIVOS DE NEURO-PSIQUIATRIA 59(1):83-88 Boy R; Correia PS; Llerena JC; Machado-Ferreira MD; Pimentel MMG Fragile X syndrome confirmed by molecular analysis: a case-control study with pre and post-puberal patients | 0 | 0 |
| 2167 | 0 | 0 | 1999 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 2168 | 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 |
| 2169 | 0 | 0 | 2030 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| 2170 | 0 | 1 | 2031 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(5):337-337 Floet AW Children with fragile X syndrome: A parents' guide | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2171 | 17 | 24 | 2034 2001 JOURNAL OF KOREAN MEDICAL SCIENCE 16(3):271-275 Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK Molecular screening for Fragile X syndrome in mentally handicapped children in Korea | 0 | 0 |
| 2172 | 0 | 0 | 2036 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; Jacobs P; Davies K; Murphy KC; Murphy DGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2173 | 0 | 0 | 2037 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 2174 | 0 | 0 | 2038 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 2175 | 0 | 0 | 2039 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 2176 | 11 | 17 | 2042 2001 MEDICAL PRINCIPLES AND PRACTICE 10(2):73-78 Alkhalaf M; Verghese L; Mushtaq SK Cytogenetic and immunohistochemical characterization of fragile X syndrome in a Kuwaiti family: Rapid antibody test for the diagnosis of mental retardation patients | 0 | 0 |
| 2177 | 0 | 2 | 2045 2001 MONATSSCHRIFT KINDERHEILKUNDE 149(3):264-264 Gladtke E Trimethoprim in the fragile X syndrome? | 0 | 0 |
| 2178 | 0 | 0 | 2046 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| 2179 | 5 | 18 | 2057 2001 REVISTA DE NEUROLOGIA 33:S6-S9 Glover G; Bernabe MJ; Carbonell P Gnosis of fragile X syndrome | 0 | 0 |
| 2180 | 19 | 22 | 2058 2001 REVISTA DE NEUROLOGIA 33:S9-S13 Ramos-Fuentes FJ New methods for the diagnosis of fragile X syndrome: A study of the FMRP in blood and hair | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2181 | 21 | 30 | 2059 2001 REVISTA DE NEUROLOGIA 33:S14-S19 Tejada MI Prevention of fragile X syndrome by prenatal genetic diagnosis: Advantages and controversial aspects | 0 | 0 |
| 2182 | 8 | 25 | 2060 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
| 2183 | 3 | 19 | 2063 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| 2184 | 2 | 12 | 2064 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 2185 | 15 | 42 | 2065 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 2186 | 61 | 105 | 2066 2001 REVISTA DE NEUROLOGIA 33:S51-S57 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behaviour relationships | 0 | 0 |
| 2187 | 12 | 29 | 2067 2001 REVISTA DE NEUROLOGIA 33:S62-S65 Chiurazzi P; Neri G Experimental therapy: Reactivation of the FMR1 gene involved in fragile X syndrome | 0 | 0 |
| 2188 | 3 | 52 | 2068 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; Pomponi MG; Tabolacci E; Torrioli MG; Vernacotola S; Neri G L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 2189 | 8 | 40 | 2069 2001 REVISTA DE NEUROLOGIA 33:S70-S76 de Diego-Otero Y Experimental therapeutic models for fragile X syndrome | 0 | 0 |
| 2190 | 0 | 7 | 2070 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2191 | 0 | 7 | 2071 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| 2192 | 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 |
| 2193 | 16 | 28 | 2077 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 0 | 0 |
| 2194 | 0 | 0 | 2078 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):175-175 Jin P; Zhang F; Zarnescu DC; Moses K; Lucchesi JC; Nichol K; Pearson CE; Warren ST A Drosophila model of fragile X premutation: CGG repeat instability and dominant-negative effects of premutation riboCGG repeat. | 0 | 0 |
| 2195 | 0 | 0 | 2080 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):259-259 Hagerman PJ; Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio R; Jacquement S; Gane L; Leehey M Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. | 0 | 0 |
| 2196 | 0 | 0 | 2081 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):270-270 Griffin KJ; Bei T; Meck J; Wong LJ; Bondy C; Stratakis CA Gender ambiguity and fragile X: a new syndrome. | 0 | 0 |
| 2197 | 0 | 0 | 2082 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):287-287 Hagerman R; Goodlin-Jones BL; Spence S; Albrect L; Bacalman S; Tassone F; Gane LW; Harris SW; Hagerman PJ The fragile X premutation and autistic spectrum disorders. | 0 | 0 |
| 2198 | 0 | 0 | 2083 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):288-288 Harris SW; Goodlin-Jones BL; Bacalman S; Jardini T; Rao S; Hagermann RJ Fragile X and autism diagnosis by two standard methodologies. | 0 | 0 |
| 2199 | 0 | 0 | 2084 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):331-331 Tassone F; Sahota P; Pleasant N; Laird C; Hagerman P Methylation analysis of the promoter region in fragile X males with hypermethylated, full mutation alleles | 0 | 0 |
| 2200 | 0 | 0 | 2085 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; Ding XD; Gargano AD; Crawford L; Gitcho N; Spence SJ; Geschwind DH; Agre Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
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