| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 15: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1401 | 0 | 0 | 8 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107 HOWARDPEEBLES PN; FINLEY WH TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 1402 | 0 | 0 | 9 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122 SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1403 | 0 | 0 | 15 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| 1404 | 0 | 0 | 32 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1405 | 0 | 0 | 33 1981 PEDIATRIC RESEARCH 15(4):645-645 PUESCHEL SM; HAYS R; MENDOZA T A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME | 1 | 1 |
| 1406 | 0 | 0 | 39 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93 HAVKIN S; CHAKI R; GOLDMAN B FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1407 | 0 | 0 | 40 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103 NOLIN S; BROWN T; JENKINS E FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING | 1 | 1 |
| 1408 | 0 | 0 | 42 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A121-A121 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; ANDERSON J FRAGILE X-LINKED MENTAL-RETARDATION - EFFECT OF AGE AND INTELLIGENCE ON EXPRESSION OF FRAGILE-X | 1 | 1 |
| 1409 | 0 | 0 | 45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131 KNOLL J; CHUDLEY AE; GERRARD JW EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1410 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 0 | 0 | 57 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1412 | 1 | 5 | 58 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| 1413 | 0 | 0 | 82 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY | 1 | 1 |
| 1414 | 0 | 21 | 85 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1415 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 1416 | 0 | 0 | 121 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 1417 | 0 | 0 | 122 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X | 1 | 1 |
| 1418 | 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 |
| 1419 | 1 | 5 | 253 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 1420 | 0 | 0 | 261 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 3 | 6 | 267 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1422 | 3 | 5 | 288 1985 HUMAN GENETICS 71(2):182-182 PEMBREY ME; WINTER RM FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 1 | 1 |
| 1423 | 2 | 3 | 289 1985 HUMAN GENETICS 71(2):183-183 SHERMAN SL; JACOBS PA; MORTON NE FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES - REPLY | 1 | 1 |
| 1424 | 2 | 2 | 295 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 1 | 1 |
| 1425 | 1 | 6 | 301 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):239-240 HAGERMAN RJ; JACKSON AW AUTISM OR FRAGILE-X SYNDROME | 0 | 1 |
| 1426 | 1 | 7 | 314 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328 HAGERMAN RJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY | 1 | 1 |
| 1427 | 0 | 0 | 355 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):186-187 DAR H; BAREL H; JAFFE M; WINTER ST THE FRAGILE-X SYNDROME - THE DILEMMA OF SELECTING PATIENTS FOR EXAMINATION | 0 | 1 |
| 1428 | 16 | 37 | 370 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 1429 | 0 | 0 | 375 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES | 1 | 1 |
| 1430 | 1 | 1 | 413 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602 HAGERMAN RJ POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 10 | 29 | 433 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1432 | 12 | 23 | 439 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122 LIN MS; SHIMANUKI K; WILSON MG EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS | 1 | 1 |
| 1433 | 0 | 0 | 474 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640 SENIOR J; KILPATRICK M; WEBB T COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME | 1 | 1 |
| 1434 | 0 | 0 | 475 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 1435 | 2 | 4 | 477 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85 COWIE VA; SINGH KR; WHEATER R; BIRD J THE FRAGILE-X SYNDROME IN TWIN SISTERS | 1 | 1 |
| 1436 | 4 | 4 | 485 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1437 | 0 | 1 | 486 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 1438 | 0 | 0 | 487 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1439 | 0 | 0 | 490 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| 1440 | 0 | 0 | 501 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 0 | 0 | 506 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):25-25 TOMMERUP N; REINTOFT I; RESKENIELSEN E; BRONDUMNIELSEN K; MIKKELSEN M UNSUSPECTED PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 0 | 1 |
| 1442 | 195 | 429 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| 1443 | 1 | 3 | 520 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| 1444 | 1 | 3 | 536 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 1445 | 6 | 13 | 570 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| 1446 | 10 | 48 | 588 1988 HUMAN GENETICS 79(4):341-346 VANDAMME B; LIEBAERS I; HENS L; BERNHEIM JL; ROOBOL C THE ROLE OF FLUORINATED PYRIMIDINE ANALOGS IN THE INDUCTION OF THE INVITRO EXPRESSION OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1447 | 27 | 63 | 608 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763 FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 1448 | 0 | 0 | 610 1988 ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM 43(6):451-454 STEINBICKER V; SEEMANOVA E; MISSBACH D THE SYNDROME OF THE FRAGILE X (MARTIN-BELL-SYNDROME MBS) | 0 | 1 |
| 1449 | 0 | 0 | 611 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME | 1 | 1 |
| 1450 | 2 | 10 | 632 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 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 | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 0 | 0 | 634 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; PETTERSSON U ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 1452 | 0 | 0 | 635 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| 1453 | 0 | 0 | 637 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; SCHWARTZ CE; HAGERMAN R; DAVIES KE GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 1454 | 0 | 0 | 657 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 1455 | 21 | 41 | 661 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 1456 | 2 | 3 | 665 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME | 1 | 1 |
| 1457 | 6 | 13 | 693 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 1458 | 1 | 4 | 714 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1459 | 2 | 3 | 729 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1460 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):173-185 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X, AND RELATED SUBJECTS .5. (1991) | 0 | 1 |
| 1462 | 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 |
| 1463 | 7 | 20 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME | 1 | 1 |
| 1464 | 14 | 31 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; ROMANO V; BOSCO P; CERATTO N; PETTERSSON U; DAHL N LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 1465 | 13 | 23 | 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; DOBKIN C CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 1466 | 1 | 7 | 809 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 1467 | 2 | 33 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; SCHWARTZRICHSTEIN C; HONG G; BROWN WT DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 1468 | 1 | 8 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; BROWN WT SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 1469 | 16 | 38 | 835 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 1470 | 5 | 13 | 836 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 4 | 13 | 843 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1472 | 0 | 0 | 847 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| 1473 | 2 | 9 | 849 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 0 | 1 |
| 1474 | 6 | 9 | 869 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST | 1 | 1 |
| 1475 | 8 | 14 | 904 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| 1476 | 8 | 19 | 905 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(6):835-838 RAMOS FJ; EMANUEL BS; SPINNER NB FREQUENCY OF THE COMMON FRAGILE SITE AT XQ27.2 UNDER CONDITIONS OF THYMIDYLATE STRESS - IMPLICATIONS FOR CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 1 |
| 1477 | 10 | 14 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; LELE K; LI SY; KRAWCZUN MS FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME | 1 | 1 |
| 1478 | 11 | 21 | 922 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148 FISCH GS; FRYNS JP FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES | 1 | 1 |
| 1479 | 12 | 19 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION | 1 | 1 |
| 1480 | 4 | 6 | 927 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173 SHAPIRO LR; WILMOT PL; FISCH GS PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 11 | 12 | 929 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):181-186 MURPHY PD; WILMOT PL; SHAPIRO LR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - RESULTS FROM PARALLEL MOLECULAR AND CYTOGENETIC STUDIES | 1 | 1 |
| 1482 | 7 | 22 | 942 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319 CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27 | 1 | 1 |
| 1483 | 5 | 5 | 946 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):339-344 VIANNAMORGANTE AM; OTTO PA NOTES ON THE POPULATION-GENETICS OF FRAGILE X SYNDROME | 1 | 1 |
| 1484 | 1 | 12 | 949 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):505-509 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; PISCHEDDA MP; SPINICCI G; MARROSU MG; FILIPPI G NEUROPSYCHOLOGICAL STUDIES IN FAMILIES WITH FRAGILE-X NEGATIVE X-LINKED MENTAL-RETARDATION | 0 | 1 |
| 1485 | 3 | 4 | 962 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477 DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P WILMS-TUMOR AND FRAGILE-X SYNDROME | 1 | 1 |
| 1486 | 5 | 11 | 966 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1487 | 16 | 24 | 974 1992 DISEASE MARKERS 10(1):1-5 KNIGHT SJL; HIRST MC; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 1 |
| 1488 | 16 | 33 | 975 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 1489 | 0 | 3 | 987 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):235-239 NATORI N A CASE OF ATYPICAL DUCHENNE TYPE MUSCULAR-DYSTROPHY WITH FRAGILE-X | 0 | 1 |
| 1490 | 7 | 8 | 993 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 19 | 25 | 996 1992 JOURNAL OF PEDIATRICS 121(3):385-390 POTTER NT; LOZZIO CB; ANDERSON IJ; BOWLIN ES; MATTESON KJ USE OF A MOLECULAR GENETIC APPROACH TO DIAGNOSING THE FRAGILE-X GENOTYPE | 1 | 1 |
| 1492 | 17 | 25 | 1002 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 1493 | 19 | 26 | 1018 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 1494 | 4 | 9 | 1019 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 1495 | 0 | 0 | 1030 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; MATHEW C; MORNET E; MADDALENA A; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES | 1 | 1 |
| 1496 | 0 | 0 | 1033 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144 HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; SEYDEL C; MAZZOCCO M; TAYLOR A HIGH-FUNCTIONING FRAGILE X MALES | 1 | 1 |
| 1497 | 0 | 0 | 1036 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448 HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; STEIN C; ZEESMAN S; CHITAYAT D; TESHIMA I; BROWN C; WARREN ST THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE | 1 | 1 |
| 1498 | 0 | 0 | 1067 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME | 1 | 1 |
| 1499 | 11 | 29 | 1095 1993 HUMAN GENETICS 92(4):373-378 MORNET E; BOGYO A; DELUCHAT C; SIMONBOUY B; MATHIEU M; THEPOT F; GRISARD MC; LEGUERN E; BOUE J; BOUE A MOLECULAR ANALYSIS OF A RING CHROMOSOME-X IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1500 | 0 | 0 | 1103 1993 IRISH MEDICAL JOURNAL 86(3):92-& KEENAN E; KEANE V; RAMSEY L FRAGILE-X SYNDROME - A REVIEW | 1 | 1 |
Page 15: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
Generated by: HistCite(Vlad).
Version: 2004.08.24