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INACTIVATION CENTERS IN THE HUMAN X CHROMOSOMENAKAGOME Y.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 2; PP. 182-194; BIBL. 4 P.Article

PRIMARY AMENORRHEA WITH A NEW MOSAIC 46, XXQI/47, XXQI XP-. CONSIDERATION ON THE X ISOCHROMOSOME FORMATION AND X CHROMOSOME INACTIVATION.HALBRECHT I; SHABTAI F; KUPFERSTAIN C et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 1; PP. 63-69; ABS. ITAL. FR. ALLEM.; BIBL. 20 REF.Article

X-AUTOSOME TRANSLOCATIONS: A REVIEWSUMMITT RL; TIPTON RE; WILROY RS JR et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 219-247; BIBL. 3 P.Article

X INACTIVATION PATTERN IN AN UNBALANCED X-AUTOSOME TRANSLOCATION WITH GONADAL DYSGENESIS.GAAL M; LASZLO J.1977; HUM. HERED.; SWITZ.; DA. 1977; VOL. 27; NO 6; PP. 396-402; BIBL. 1 P.Article

DIFFERENT PATTERNS OF X CHROMOSOME INACTIVITY IN LYMPHOCYTES AND FIBROBLASTS OF A HUMAN BALANCED X; AUTOSOME TRANSLOCATIONHELLKUHL B; DE LA CHAPELLE A; GRZESCHIK KH et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 126-129; BIBL. 20 REF.Article

GONODAL AND STATURAL DETERMINANTS ON THE X CHROMOSOME AND THEIR RELATIONSHIP TO IN VITRO STUDIES SHOWING PROLONGED CELL CYCLES IN 45,X;46,X,DEL(X) (P11);46,X,DEL(X) (Q13); AND 46,X,DEL(X) (Q22) FIBROBLASTSSIMPSON JL; LEBEAU MM.1981; AM. J. OBSTET. GYNECOL.; ISSN 0002-9378; USA; DA. 1981; VOL. 141; NO 8; PP. 930-940; BIBL. 16 REF.Article

ANOMALIES DE STRUCTURE DU CHROMOSOME X CHEZ LES SUJETS DE PHENOTYPE FEMININDEVIN CATHERINE.sd; FRA; DA. S.D.; 118; 135-VII P.-PL.; 30 CM; BIBL. 91 REF.; TH.: MED./NANCY 1/1979Thesis

X-LINKED MENTAL RETARDATION WITH MACRO-ORCHIDISM AND THE FRAGILE SITE AT XQ27 OR 28SUTHERLAND GR; ASHFORTH PLC.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 117-120; BIBL. 11 REF.Article

CLINICAL AND CYTOGENETIC ASPECTS OF X-CHROMOSOME DELETIONSGOLDMAN B; POLANI PE; DAKER MG et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 1; PP. 36-52; BIBL. 3 P.Article

L'INFLUENCE DE LA PROLIFERATION CELLULAIRE SUR LA CONDENSATION DU CHROMOSOME X EN CULTURE DES INDIVIDUS A CARYOTYPE 49 XXXXXTUMBABEYA A; GUEGEN A.1979; C.R. ACAD. SCI., D; FRA; DA. 1979; VOL. 289; NO 7; PP. 579-582; ABS. ENG; BIBL. 15 REF.Article

A STUDY OF X CHROMOSOME REGULATION DURING OOGENESIS IN THE MOUSE.ANDINA RJ.1978; EXPER. CELL RES.; U.S.A.; DA. 1978; VOL. 111; NO 1; PP. 211-218; BIBL. 32 REF.Article

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

FURTHER STUDIES ON THE RIBOSOMAL RNA CISTRONS OF SCIARA COPROPHILA (DIPTERA).GERBI SA; CROUSE HV.1976; GENETICS; U.S.A.; DA. 1976; VOL. 83; NO 1; PP. 81-90; BIBL. 2 P.Article

X-CHROMOSOME POLYSOMY IN THE FEMALE: PERSONAL EXPERIENCE AND REVIEW OF THE LITERATUREFRYNS JP; KLECZKOWSKA A; PETIT P et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 5; PP. 341-349; BIBL. 2 P.Article

GENE MAPPING AND SERENDIPITY: THE LOCUS FOR TORTICOLLIS, KELOIDS, CRYPTORCHIDISM AND RENAL DYSPLASIA (31430, MCKUSICK) IS AT XQ-28 DISTAL TO THE G6GPD LOCUSZUFFARDI O; FRACCARO M.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 280-281; BIBL. 13 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

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

STUDIES OF HUMAN X-CHROMOSOME DNA.MIGEON B.1975; CARNEGIE INSTIT. WASHINGTON, YB.; U.S.A.; DA. 1975-1976; VOL. 75; PP. 22-23Article

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

X LONG ARM DELETION WITH OLIGOMENORRHOEAMIJIN K; STOLEVIC E; ADZIC S et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 305-306; BIBL. 13 REF.Article

IDENTIFICATION DES EFFETS DU CHROMOSOME X PAR LA SEPARATION DES COMPOSANTES DE LA VARIANCE PHENOTYPIQUEAGEEV SV.1982; GENETIKA; ISSN 0016-6758; SUN; DA. 1982; VOL. 18; NO 7; PP. 1149-1160; ABS. ENG; BIBL. 9 REF.Article

LATE REPLICATION PATTERNS IN ADULT AND EMBRYONIC MICE CARRYING SEARLE'S X-AUTOSOME TRANSLOCATIONDISTECHE CM; EICHER EM; LATT SA et al.1981; EXP. CELL. RES.; ISSN 0014-4827; USA; DA. 1981; VOL. 133; NO 2; PP. 357-362; BIBL. 21 REF.Article

LETTER TO THE EDITOR: MARKER X CHROMOSOME INDUCTION IN FIBROBLASTS BY FUDRTOMMERUP N; NIELSEN KB; MIKKELSEN M et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 263-264Article

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

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