FRAGILE X CHROMOSOME IN NORMAL MALES. REPLYDAKER MG; HECHT F; JACKY PB et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 795-797; BIBL. 5 REF.Article

BRDU-SENSITIVE FRAGILE SITE ON LONG ARM OF CHROMOSOME 16CROCI G.1983; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1983; VOL. 35; NO 3; PP. 530-533; BIBL. 10 REF.Article

CHROMOSOMAL INSTABILITY IN ATAXIA TELANGIECTASIAKOHN PH; WHANG PENG J; LEVIS WR et al.1982; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1982; VOL. 6; NO 4; PP. 289-302; BIBL. 47 REF.Article

CHROMOSOME 17 HAS A REAL FRAGILE SITE AT P12SHABTAI F; KLAR D; HALBRECHT I et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 2; PP. 177-179; BIBL. 6 REF.Article

INCREASE IN THE INCIDENCE OF THE FRAGILE SITE XQ27 IN PROMETAPHASESBARBI G; STEINBACH P.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 82; BIBL. 4 REF.Article

ABSENCE DE FRA(X)Q27/Q28 DANS LE SYNDROME DE LA MICROCEPHALIE LIEE A L'XFASHINGBAUER C; ROTT HD; SCHWINGER E et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 275; BIBL. 2 REF.Article

ASPECTS GENETIQUES DES SITES FRAGILES AUTOSOMIQUES: A PROPOS DE 40 CASGUICHAOUA M; MATTEI MG; MATTEI JF et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 183-197; ABS. ENG; BIBL. 75 REF.Article

APPARENT HOMOZYGOSITY FOR THE FRAGILE SITE AT XQ28 IN A NORMAL FEMALEBRONDUM NIELSEN K; TOMMERUP N; POULSEN H et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 60-62; BIBL. 9 REF.Article

ORGAN SITE SPECIFICITY FOR CANCER IN CHROMOSOMAL INSTABILITY DISORDERSFEINBERG AP; COFFEY DS.1982; CANCER RESEARCH; ISSN 0008-5472; USA; DA. 1982; VOL. 42; NO 8; PP. 3252-3254; BIBL. 37 REF.Article

HIGH RESOLUTION BANDING AND THE LOCUS OF THE XQ FRAGILE SITEBROOKWELL R; TURNER G.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 77; BIBL. 7 REF.Article

PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOMESCHMIDT A; PASSARGE E; SEEMANOVA E et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 285-286; BIBL. 13 REF.Article

SCREENING FOR FRA(X)(Q) IN A POPULATION OF MENTALLY RETARDED MALESFROSTER ISKENIUS U; FELSCH G; SCHIRREN C et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 2; PP. 153-157; BIBL. 27 REF.Article

HERITABLE FRAGILE SITES ON HUMAN CHROMOSOMES. IX: POPULATION CYTOGENETICS AND SEGREGATION ANALYSIS OF THE BRDU-REQUIRING FRAGILE SITE AT 10925SUTHERLAND GR.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 5; PP. 753-756; BIBL. 7 REF.Article

MITOTIC RECOMBINATION AND SEGREGATION OF SATELLITIS IN BLOOM'S SYNDROMETHERMAN E; OTTO PG; SHAHIDI NT et al.1981; CHROMOSOMA; ISSN 0009-5915; DEU; DA. 1981; VOL. 82; NO 5; PP. 627-636; BIBL. 15 REF.Article

LES SYNDROMES D'INSTABILITE CHROMOSOMIQUEGERMAIN D; BERNHEIM A.1982; PATHOL.-BIOL.; ISSN 0031-3009; FRA; DA. 1982; VOL. 30; NO 9; PP. 802-816; ABS. ENG; BIBL. 173 REF.Article

HERITABLE FRAGILE SITES ON HUMAN CHROMOSOMES. II: DISTRIBUTION, PHENOTYPIC EFFECTS, AND CYTOGENETICSSUTHERLAND GR.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 2; PP. 136-148; BIBL. 31 REF.Article

FRAGILE X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC CELL HYBRIDIZATIONBRYANT EM; MARTIN GM; HOEHN H et al.1983; CYTOGENETICS AND CELL GENETICS; ISSN 0301-0171; CHE; DA. 1983; VOL. 35; NO 3; PP. 223-225; BIBL. 10 REF.Article

L'ARRIERATION MENTALE AVEC FRAGILITE DE L'X: ARMENFRAX. REVUE ET ETUDES PERSONNELLESENGEL E.1983; REVUE MEDICALE DE LA SUISSE ROMANDE; ISSN 0035-3655; CHE; DA. 1983; VOL. 103; NO 4; PP. 333-344; BIBL. 80 REF.Article

A TEMPERATURE SENSITIVE MUTANT OF A CHINESE HAMSTER CELL LINE EXHIBITING HIGH CHROMOSOMAL BREAKAGEFAINSOD A; VOSS R; SPANN P et al.1983; CYTOGENETICS AND CELL GENETICS; ISSN 0301-0171; CHE; DA. 1983; VOL. 35; NO 2; PP. 104-109; BIBL. 20 REF.Article

MARKER X-ASSOCIATED MENTAL RETARDATION: A STUDY OF 150 RETARDED MALESKAHKONEN M; LEISTI J; WILSKA W et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 6; PP. 397-404; BIBL. 27 REF.Article

A NEW HERITABLE FRAGILE SITE ON HUMAN CHROMOSOME 3RUDDUCK C; FRANZEN G.1983; HEREDITAS; ISSN 0018-0661; SWE; DA. 1983; VOL. 98; NO 2; PP. 297-299; BIBL. 14 REF.Article

L'ENCEPHALOPATHIE LIEE A LA FRAGILITE DU CHROMOSOME XMATTEI JF.1982; ARCHIVES FRANCAISES DE PEDIATRIE; ISSN 0003-9764; FRA; DA. 1982; VOL. 39; NO 8; PP. 633-639; BIBL. 81 REF.Article

THE FRAGILE X CHROMOSOME IN A LARGE INDIAN KINDREDGARDNER RJM; SMART RD; CORNELL JM et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 4; PP. 311-317; BIBL. 14 REF.Article

A NEW INDUCIBLE FRAGILE SITE ON CHROMOSOME 3(P 14.2) IN HUMAN LYMPHOCYTESWEGNER RD.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 3; PP. 297-298; BIBL. 11 REF.Article

MARTIN-BELL SYNDROME FRA(X) (Q28) IN A SRI LANKAN FAMILYPRIYANI SOYSA; MANO SENANAYAHE; MIKKELSEN M et al.1982; JOURNAL OF MENTAL DEFICIENCY RESEARCH; ISSN 0022-264X; GBR; DA. 1982; VOL. 26; NO 4; PP. 251-257; BIBL. 18 REF.Article