HistCite - Fragile-X

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#	Date / Author / Journal	LCS	GCS	LCR	CR
1601	502 FANTES J, GOSDEN J, PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X CYTOGENETICS AND CELL GENETICS. 1988; 48 (3): 142-147	0	4	6	24
1602	617 SAUER SM, PHELAN MC, RICHER CL, SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA CYTOGENETICS AND CELL GENETICS. 1989; 50 (2-3): 172-173	1	1	2	10
1603	618 DAHL N, MALMSTROM H, HAMMARSTROMHEEROMA K, WADELIUS C, GUSTAVSON KH, et al. ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 982-982	0	3	0	0
1604	619 GOONEWARDENA P, GROSS AC, FERRANDO CJ, BROWN T, DAHL N, et al. ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1007-1007	0	1	0	0
1605	620 GROSS AC, FERRANDO CJ, BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1009-1009	0	1	0	0
1606	621 SUTHERLAND GR, BAKER E THE COMMON FRAGILE SITE (FRAXD) IS AT XQ27.2 AND CAN BE DISTINGUISHED FROM THE FRAGILE-X (FRAXA) AT XQ27.3 CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1086-1087	2	8	0	0
1607	622 THIBODEAU SN, SCHAID D, BREN G, BLOOMFIELD J, BELL MV, et al. GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1089-1090	0	1	0	0
1608	623 WAHLSTROM J, WITTENGERSTROM I, ANVRET M, ODEN A, JOHANNESSON T, et al. RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1100-1101	0	2	0	1
1609	747 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES CYTOGENETICS AND CELL GENETICS. 1991; 56 (3-4): 221-221	0	0	0	2
1610	748 SHAPIRO LR, EALLONARDO SJ, WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED CYTOGENETICS AND CELL GENETICS. 1991; 56 (3-4): 221-221	1	1	0	0
#	Date / Author / Journal	LCS	GCS	LCR	CR
1611	749 BOUVET A, BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2054-2055	1	1	2	9
1612	750 DIETRICH A, LANGENSTEIN G, TONIOLO D, WARREN ST, LEHRACH H, et al. A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2062-2062	0	0	0	2
1613	751 DJABALI M, NGUYEN C, BIUNNO I, IKEDA JE, OOSTRA BA, et al. LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2062-2062	0	0	0	0
1614	752 GRAHAM CA, GRIER DG, CLARKSON M, STEWART FJ, NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2065-2065	0	0	2	5
1615	753 HIRST M, NAKAHORI Y, KNIGHT S, ROCHE A, RAUT C, et al. A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2067-2067	0	0	2	5
1616	754 LYNCH M, KREMER EJ, PRITCHARD MA, YU S, BAKER E, et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2076-2076	0	0	0	0
1617	755 POUSTKA A, DIETRICH A, KIOSCHIS P, KORN B, GROSS B, et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2082-2082	0	0	0	4
1618	756 RIGGINS GJ, SHERMAN SL, OOSTRA BA, FEITELL D, SUTCLIFFE JS, et al. A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE CYTOGENETICS AND CELL GENETICS. 1991; 58 (3-4): 2085-2085	1	2	1	3
1619	964 SHAPIRO LR, WILMOT PL, ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE CYTOGENETICS AND CELL GENETICS. 1992; 60 (3-4): 265-265	0	0	0	0
1620	965 JACKY PB, JENKINS EC FRAGILE-X CYTOGENETIC GUIDELINES REVIEWED - RELEVANCE TO FRA(X) MOLECULAR GENETIC-STUDIES AND TO APPROPRIATENESS OF CHROMOSOME-STUDIES IN ALL CASES OF DEVELOPMENTAL DELAY - A DISCUSSION CYTOGENETICS AND CELL GENETICS. 1992; 60 (3-4): 266-266	0	0	0	0
#	Date / Author / Journal	LCS	GCS	LCR	CR
1621	1085 LUTHARDT F, SKOGERBOE K, SHADOAN P, DINNO N IDENTIFICATION OF DE-NOVO DEL(Y)(Q11.23) IN A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE USING A Y-CHROMOSOME COCKTAIL PROBE (DYZ1, DYZ3) CYTOGENETICS AND CELL GENETICS. 1993; 63 (4): 252-252	0	0	0	0
1622	1086 OSTROWSKI RS, GRASS FS, LOVETTJELLEMA J AN INVESTIGATION OF THE FRAGILE-X SITE AS IT RELATES TO CHROMOSOME OVERLAP IN CULTURED HUMAN WHITE BLOOD-CELLS CYTOGENETICS AND CELL GENETICS. 1993; 63 (4): 254-254	0	0	0	0
1623	1087 JACKY PB, BERRY TL, LAMB OA, LANGLOIS MI, OLSON CL, et al. ARE FRAGILE-X CHROMOSOME-STUDIES DEAD CYTOGENETICS AND CELL GENETICS. 1993; 63 (4): 256-256	0	0	0	0
1624	1088 SCHMIDT M X-CHROMOSOME INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE X-REGION CYTOGENETICS AND CELL GENETICS. 1993; 64 (3-4): 187-187	0	0	1	1
1625	1349 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST CYTOGENETICS AND CELL GENETICS. 1995; 69 (1-2): 116-116	0	0	0	0
1626	1651 Malarchuk S, Li S, Wertelecki W, Bychkova A, Livshits L Analysis of patients with fragile X syndrome in Ukraine. CYTOGENETICS AND CELL GENETICS. 1997; 77 (1-2): P250-P250	0	0	0	0
1627	1652 Tengstrom C, Ikonen A, Kaski M, Autio S High resolution banding and fragile X - screening in persons with mild mental retardation. CYTOGENETICS AND CELL GENETICS. 1997; 77 (1-2): P287-P287	0	0	0	0
1628	1880 Arrieta I, Criado B, Martinez B, Telez M, Fiores P, et al. Molecular and cytogenetic analysis of the fragile X syndrome in a sample from Basque Country: are the Basques a population with a low risk of developing the syndrome? CYTOGENETICS AND CELL GENETICS. 1999; 85 (1-2): 137-138	0	0	0	0
1629	1881 Sofocleous C, Mavrou A, Fryssira H, Kolialexi A, Tsenghi C, et al. FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece CYTOGENETICS AND CELL GENETICS. 1999; 85 (1-2): 165-165	0	0	0	0
1630	1882 Tayel SM, Al-Naggar RL, Ali FE, Al-Awadi SA Two-step fragile X screening program in mentally retarded males CYTOGENETICS AND CELL GENETICS. 1999; 85 (1-2): 167-167	0	0	0	0
#	Date / Author / Journal	LCS	GCS	LCR	CR
1631	2018 Bardoni B, Giglio S, Schenck A, Rocchi M, Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12 CYTOGENETICS AND CELL GENETICS. 2000; 89 (1-2): 11-13	2	3	1	6
1632	679 PIPER J, FANTES J, GOSDEN J, JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE CYTOMETRY. 1990; 11 (1): 73-79	0	4	1	12
1633	2564 Lee A, Li WJ, Xu KY, Bogert BA, Su K, et al. Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 DEVELOPMENT. 2003 NOV; 130 (22): 5543-5552	33	73	25	62
1634	3226 Tessier CR, Broadie K Drosophila fragile X mental retardation protein developmentally regulates activity-dependent axon pruning DEVELOPMENT. 2008 APR 15; 135 (8): 1547-1557	7	12	54	92
1635	3284 Gatto CL, Broadie K Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure DEVELOPMENT. 2008 AUG 1; 135 (15): 2637-2648	4	5	36	67
1636	2530 Reiss AL, Dant CC The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies DEVELOPMENT AND PSYCHOPATHOLOGY. 2003 FAL; 15 (4): 927-968	25	40	153	233
1637	2769 van 't Padje S, Engels B, Blonden L, Severijnen LA, Verheijen F, et al. Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene DEVELOPMENT GENES AND EVOLUTION. 2005 APR; 215 (4): 198-206	5	6	25	33
1638	2505 Qin M, Kang J, Smith CB Increased local rates of cerebral protein synthesis in fragile X knockout mice. DEVELOPMENTAL BIOLOGY. 2003 JUL 15; 259 (2): 528-529	0	0	0	0
1639	2651 Zhang YQ, Matthies HJG, Mancuso J, Andrews HK, Woodruff E, et al. The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis DEVELOPMENTAL BIOLOGY. 2004 JUN 15; 270 (2): 290-307	12	25	18	58
1640	2943 Olechowicz SL, Miller JN, Warren JT Analysis of the in vivo function of the zebrafish fragile X gene family DEVELOPMENTAL BIOLOGY. 2006 JUL 1; 295 (1): 351-351	0	0	0	0
#	Date / Author / Journal	LCS	GCS	LCR	CR
1641	3267 Monzo K, Dowd SR, Minden JS, Sisson JC Proteomic analysis of Drosophila fragile X mutant cleavage stage embryos DEVELOPMENTAL BIOLOGY. 2008 JUL 15; 319 (2): 519-520	0	0	0	0
1642	3449 Epstein AM, Bauer CR, Ho A, Bosco G, Zarnescu DC Drosophila Fragile X Protein controls cellular proliferation by regulating cbl levels in the ovary DEVELOPMENTAL BIOLOGY. 2009 JUN 1; 330 (1): 83-92	0	0	21	37
1643	1254 HAGERMAN RJ, FULTON MJ, LEAMAN A, RIDDLE J, HAGERMAN K, et al. A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME DEVELOPMENTAL BRAIN DYSFUNCTION. 1994 MAR-JUN; 7 (2-3): 155-164	21	25	19	64
1644	1396 Hagerman R, Staley L, Brown WT, Taylor A, Meadow K, et al. Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 167-184	0	0	9	23
1645	1397 Nommensen D Report of the Executive Director of the National Fragile X Foundation DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 185-186	0	0	0	0
1646	1398 Abrams MT, Reiss AL Quantitative brain imaging studies of fragile X syndrome DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 187-198	2	3	32	75
1647	1399 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 199-217	5	5	47	131
1648	1400 Musumeci SA, Ferri R, Elia M, DalGracco S, Scuderi C, et al. Sleep neurophysiology in fragile X patients DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 218-222	4	5	3	16
1649	1401 King RA, Hagerman R, Houghton M Ocular findings in fragile X syndrome DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 223-229	3	3	10	22
1650	1402 Brun C, Obiols JE, Cheema A, OConnor R, Riddle J, et al. Longitudinal IQ changes in fragile X females DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 230-241	1	2	27	36
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1651	1403 Freund LS, Peebles CD, Aylward E, Reiss AL Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 242-251	19	26	17	33
1652	1404 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 252-269	29	31	40	75
1653	1405 Belser RC, Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 270-279	37	45	15	38
1654	1406 Sobesky WE, Porter D, Pennington BF, Hagerman RJ Dimensions of shyness in fragile X females DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 280-292	18	23	19	37
1655	1407 Jenkins EC, Houck GE, Ding XH, Li SY, StarkHouck SL, et al. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 293-301	1	1	26	41
1656	1408 Holden JJA, Chalifoux M, Wing M, JulienInalsingh C, Scott E, et al. Distribution and frequency of FMR1 CGG repeat number in institutionalized developmentally disabled individuals DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 302-309	0	3	18	26
1657	1409 Wake SA, Robinson H Assessment of counselling of normal males and normal transmitting male carriers identified in fragile X families DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 319-326	0	0	12	21
1658	1410 Roy JC, Johnsen J, Breese K, Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 327-335	6	10	10	25
1659	1411 Hagerman RJ, Riddle JE, Roberts LS, Breese K, Fulton M Survey of the efficacy of clonidine in fragile X syndrome DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 336-344	15	15	8	35
1660	1412 Rattazzi MC Protein therapy in fragile X syndrome - A brief overview of principles, potentials and problems DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 345-352	0	0	2	23
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1661	1413 Lin JFH Introduction to fragile X syndrome for parents DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 359-362	0	0	0	7
1662	1414 Glass L Females with fragile X: A parent's perspective DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 363-366	0	0	0	0
1663	1415 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 370-379	0	0	6	9
1664	1416 McConkieRosell A, Robinson H, Wake S, Staley L, Heller K, et al. Educating extended family members about the inheritance of the fragile X syndrome DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 390-395	0	1	0	0
1665	1417 Mazzocco MMM, Lachiewicz AM, Kovar CG, Freund LS, Baumgardner TL, et al. Psychological and emotional studies of the fragile X mutation - A workshop summary DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 396-404	0	0	7	18
1666	1418 Holden JJA, Chalifoux M, Wing M, JulienInalsingh C, Lawson JS, et al. Distribution and frequency of FMR1 CGG repeat numbers in the general population DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 405-407	6	13	7	8
1667	1419 HowardPeebles PN, Maddalena A, Black SH, Levinson G, Bick DP, et al. Fragile X screening in pediatric and obstetrical patients DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 408-410	2	2	5	9
1668	1420 [Anon] 4th International Fragile X and X-Linked Mental Retardation Conference - Albuquerque, NM, USA, June 8-12, 1994 - Abstracts DEVELOPMENTAL BRAIN DYSFUNCTION. 1995 JUL-DEC; 8 (4-6): 411-416	0	0	0	0
1669	2795 Galvez R, Smith RL, Greenough WT Olfactory bulb mitral cell dendritic pruning abnormalities in a mouse model of the Fragile-X mental retardation syndrome: Further support for FMRP's involvement in dendritic development DEVELOPMENTAL BRAIN RESEARCH. 2005 JUN 30; 157 (2): 214-216	1	4	8	14
1670	2739 Zarnescu DC, Jin P, Betschinger J, Nakamoto M, Wang Y, et al. Fragile X protein functions with Lgl and the PAR complex in flies and mice DEVELOPMENTAL CELL. 2005 JAN; 8 (1): 43-52	13	29	17	52
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1671	2760 Costa A, Wang Y, Dockendorff TC, Erdjument-Bromage H, Tempst P, et al. The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway DEVELOPMENTAL CELL. 2005 MAR; 8 (3): 331-342	11	22	10	43
1672	3243 Dictenberg JB, Swanger SA, Antar LN, Singer RH, Bassell GJ A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome DEVELOPMENTAL CELL. 2008 JUN; 14 (6): 926-939	10	31	17	52
1673	3356 Murphy MM A REVIEW OF MATHEMATICAL LEARNING DISABILITIES IN CHILDREN WITH FRAGILE X SYNDROME DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. 2009; 15 (1): 21-27	1	5	29	47
1674	3357 Schneider A, Hagerman RJ, Hessl D FRAGILE X SYNDROME-FROM GENES TO COGNITION DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. 2009; 15 (4): 333-342	0	0	80	116
1675	3358 Lightbody AA, Reiss AL GENE, BRAIN, AND BEHAVIOR RELATIONSHIPS IN FRAGILE X SYNDROME: EVIDENCE FROM NEUROIMAGING STUDIES DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. 2009; 15 (4): 343-352	0	0	53	75
1676	3359 Hall SS TREATMENTS FOR FRAGILE X SYNDROME: A CLOSER LOOK AT THE DATA DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. 2009; 15 (4): 353-360	0	0	29	48
1677	3467 Hamada A, Miyawaki K, Honda-sumi E, Tomioka K, Mito T, et al. Loss-of-Function Analyses of the Fragile X-Related and Dopamine Receptor Genes by RNA Interference in the Cricket Gryllus bimaculatus DEVELOPMENTAL DYNAMICS. 2009 AUG; 238 (8): 2025-2033	0	0	6	39
1678	2576 Abbeduto L, Murphy MM Language, social cognition, maladaptive behavior, and communication in Down Syndrome and fragile X syndrome DEVELOPMENTAL LANGUAGE DISORDERS: FROM PHENOTYPES TO ETIOLOGIES. 2004; : 77-97	0	15	10	46
1679	2577 Bailey DB, Roberts JE, Hooper SR, Hatton DD, Mirrett PL, et al. Research on Fragile X Syndrome and autism: Implications for the study of genes, environments, and developmental language disorders DEVELOPMENTAL LANGUAGE DISORDERS: FROM PHENOTYPES TO ETIOLOGIES. 2004; : 121-150	0	9	67	144
1680	60 SERGOVICH F, POZSONYI J, HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1982; 24 (2): 252-253	1	1	0	0
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1681	275 PUESCHEL SM, FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1985; 27 (1): 95-96	0	0	0	0
1682	404 GILLBERG C, WAHLSTROM J, JOHANSSON R, TORNBLOM M, ALBERTSSONWIKLAND K FOLIC-ACID AS AN ADJUNCT IN THE TREATMENT OF CHILDREN WITH THE AUTISM FRAGILE-X SYNDROME (AFRAX) DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1986 OCT; 28 (5): 624-627	8	18	2	9
1683	495 THAKE A, TODD J, WEBB T, BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1987 DEC; 29 (6): 711-719	12	16	9	27
1684	523 HO HZ, GLAHN TJ, HO JC THE FRAGILE-X SYNDROME DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1988 APR; 30 (2): 257-261	2	3	21	37
1685	601 CAMMARATA S, ARCHIDIACONO N, ROMEO G, BENASSI G, GUARINO M, et al. PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1988 OCT; 30 (5): 646-649	1	3	2	13
1686	858 FERRIER LJ, BASHIR AS, MERYASH DL, JOHNSTON J, WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1991 SEP; 33 (9): 776-788	34	41	12	47
1687	1066 GOLDSON E, HAGERMAN RJ THE FRAGILE-X SYNDROME DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1992 SEP; 34 (9): 826-832	3	4	23	48
1688	1128 BARNICOAT AJ, DOCHERTY Z, BOBROW M WHERE HAVE ALL THE FRAGILE-X BOYS GONE DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1993 JUN; 35 (6): 532-539	4	6	16	28
1689	1801 Gringras P, Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1998 JAN; 40 (1): 62-64	1	3	12	14
1690	1973 Hatton DD, Bailey DB, Hargett-Beck MQ, Skinner M, Clark RD Behavioral style of young boys with fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 1999 SEP; 41 (9): 625-632	18	24	13	65
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1691	2161 Sheldon L, Turk J Monozygotic boys with fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2000 NOV; 42 (11): 768-774	2	3	23	46
1692	2189 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2001 FEB; 43 (2): 142-142	0	0	0	1
1693	2425 Berry-Kravis E Epilepsy in fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2002 NOV; 44 (11): 724-728	22	32	17	25
1694	2753 Weiskop S, Richdale A, Matthews J Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2005 FEB; 47 (2): 94-104	7	18	1	33
1695	2918 Wouters H, Fonteyne A, Lagae L, Stiers P Specific memory impairment in a multiple disabled male with fragile X syndrome and temporal lobe epilepsy DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2006 MAY; 48 (5): 378-382	0	0	4	23
1696	2934 Wouters Specific memory impairment in a multiple disabled male with fragile X syndrome and temporal lobe epilepsy (vol 48, pg 378, 2006) DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2006 JUL; 48 (7): 624-624	0	0	0	1
1697	2951 Miller-Horn J, Herzog K, Kothare SV Cyanotic episodes in a male child with fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2006 AUG; 48 (8): 690-692	0	0	5	21
1698	3468 Enticott PG White matter integrity in frontostriatal pathways and neurocognition in fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2009 AUG; 51 (8): 576-576	0	0	2	3
1699	3469 Haas BW, Barnea-Goraly N, Lightbody AA, Patnaik SS, Hoeft F, et al. Early white-matter abnormalities of the ventral frontostriatal pathway in fragile X syndrome DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2009 AUG; 51 (8): 593-599	2	2	7	25
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620 GROSS AC, FERRANDO CJ, BROWN WT

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CYTOGENETICS AND CELL GENETICS. 1989; 51 (1-4): 1009-1009

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621 SUTHERLAND GR, BAKER E

THE COMMON FRAGILE SITE (FRAXD) IS AT XQ27.2 AND CAN BE DISTINGUISHED FROM THE FRAGILE-X (FRAXA) AT XQ27.3

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752 GRAHAM CA, GRIER DG, CLARKSON M, STEWART FJ, NEVIN NC

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1398 Abrams MT, Reiss AL

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1403 Freund LS, Peebles CD, Aylward E, Reiss AL

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Anterior to posterior limb of the internal capsule morphology in fragile X syndrome

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. 2009 OCT; 51 (10): 839-840

Fragile-X Papers with one of the following phrases in the title: fragile x or FMRP or trinucleotide expansion or nucleotide expansion or cgg	Historiographs	Glossary HistCite Guide About Grand Totals: LCS 37096, GCS 67698, CR 85479 Collection span: 1967 - 2010
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