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CHROMOSOMAL MAPPING OF THE SIMIAN SARCOMA VIRUS ONC GENE ANALOGUE IN HUMAN CELLSSWAN DC; MCBRIDE OW; ROBBINS KC et al.1982; PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. BIOLOGICAL SCIENCES; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 15; PP. 4691-4695; BIBL. 50 REF.Article

LA SINDROME R(22). = LE SYNDROME R(22)CURATOLO P; PAOLELLA A; PORRO G et al.1978; CLIN. PEDIATR.; ITAL.; DA. 1978; VOL. 60; NO 1; PP. 10-17; ABS. ANGL.; BIBL. 11 REF.Article

CYTOGENETIC STUDIES IN TWENTY HUMAN BRAIN TUMORS: ASSOCIATION OF NO 22 CHROMOSOME ABNORMALITIES WITH TUMORS OF THE BRAINYAMADA K; KONDO T; YOSHIOKA M et al.1980; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1980; VOL. 2; NO 4; PP. 293-307; BIBL. 27 REF.Article

THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22KELLEY RI; ZACKAI EH; EMANUEL BS et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 2; PP. 197-200; BIBL. 22 REF.Article

CHROMOSOME 22 EN ANNEAU: R(22)TEYSSIER M; MOREAU N.1982; BULL. ASSOC. ANAT.; ISSN 0376-6160; FRA; DA. 1982; VOL. 66; NO 193; PP. 273-282; ABS. ENG; BIBL. 2 P.Article

TRISOMY 22 SYNDROME IN A 26-YEAR-OLD FEMALE: A FOLLOW-UP EXAMINATIONANNEREN G; GUSTAVSON KH.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 94; NO 1; PP. 67-71; BIBL. 10 REF.Article

TRISOMIE 22 PARTIELLE.TAILLEMITE JL; BAHEUX MORLIER G; VAN DEN AKKER J et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 291-293; ABS. ANGL.; BIBL. 15 REF.Article

DISCUSSION DES ELEMENTS DIAGNOSTIQUES DE LA TRISOMIE 22. A PROPOS D'UNE OBSERVATIONMURATORI BENELLI LUCIA.1980; ; FRA; DA. 1980; 57 P.; 30 CM; BIBL. 7 P.; TH.: MED./PARIS 7/1980/145Thesis

ETUDE D'UN SUJET AVEC CARYOTYPE 46, XY, 22 P+.TRABALZA N; FURBETTA M; ROSI G et al.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 2; PP. 177-184; ABS. ENG/GER; BIBL. 24 REF.Article

A CASE OF PARTIAL TRISOMY 22 WITHOUT CAT-EYE STIGMATAKADOTANI T; KATANO T; YAMAOKA H et al.1978; PROC. JAP. ACAD. B; JPN; DA. 1978; VOL. 54; NO 5; PP. 217-221; BIBL. 9 REF.Article

ASSIGNMENT OF NADH-CYTOCHROME B5 REDUCTASE (DIA1 LOCUS) TO HUMAN CHROMOSOME 22.JULIEN C; VIBERT M; WEIL D et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 233-239; BIBL. 19 REF.Article

MONOSOMY 22 WITH HUMORAL IMMUNODEFICIENCY: IS THERE AN IMMUNOGLOBULIN CHAIN DEFICIT .GARCIA MIRANDA JL; OTERO GOMEZ A; VARELA ANSEDES H et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 1; PP. 69-72; BIBL. 16 REF.Article

TWO SUCCESSIVE PARTIAL TRISOMIES FOR OPPOSITE HALVES OF CHROMOSOME 22 IN A MOTHER WITH A BALANCED TRANSLOCATIONBENDEL RP; BALDINGER S; MILLARD C et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 313; BIBL. 2 REF.Article

REGIONAL ASSIGNMENT OF ARYLSULFATASE A, MITOCHONDRIAL ACONITASE AND NADH-CYTOCHROME B5 REDUCTASE BY SOMATIC CELL HYBRIDIZATIONHORS CAYLA MC; JUNIEN C; HEUERTZ S et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 140-143; BIBL. 15 REF.Article

FELSENBEINBEFUNDE BEI DER TRISOMIE 22 = SIGNES AU NIVEAU DE L'OS TEMPORAL DANS LA TRISOMIE 22ARNOLD W; SCHUKNECHT HF; VON VOSS H et al.1981; LARYNGOL. RHINOL. OTOL.; ISSN 0340-1588; DEU; DA. 1981; VOL. 60; NO 10; PP. 545-549; ABS. ENG; BIBL. 10 REF.Article

DESCRIZIONE DI UN CASO DI TRISOMIA 21 CON TRASLOCAZIONE = DESCRIPTION D'UN CAS DE TRISOMIE 21 PAR TRANSLOCATIONGRIMOLDI MG; LAVEZZI AM.1981; FOLIA HERED. PATHOL.; ISSN 0015-5578; ITA; DA. 1981; VOL. 30; NO 2; PP. 21-25; ABS. ENG; BIBL. 5 REF.Article

ASSIGNMENT OF THE GENES FOR HUMAN 1 IMMUNOGLOBULIN CHAINS TO CHROMOSOME 22ERIKSON J; MARTINIS J; CROCE CM et al.1981; NATURE (LOND.); ISSN 0028-0836; GBR; DA. 1981; VOL. 294; NO 5837; PP. 173-175; BIBL. 18 REF.Article

CONTRIBUTION A L'ETUDE D'UN SYNDROME CLINIQUE ET CYTOGENETIQUE DE CHROMOSOME 22 EN ANNEAU: A PROPOS DE DEUX NOUVELLES OBSERVATIONSALLARD CHRISTIAN.1980; ; FRA; DA. 1980; 146; 102 P.: ILL.; 30 CM; BIBL. 94 REF.; TH.: MED./PARIS 5/1980Thesis

ASSIGNMENT OF THE DIA, LOCUS TO CHROMOSOME 22.FISHER RA; POVEY S; BOBROW M et al.1977; ANN. HUM. GENET.; G.B.; DA. 1977; VOL. 41; NO 2; PP. 151-155; BIBL. 15 REF.Article

CONTRIBUTO ALLA PATOLOGIA DEL CROMOSOMA 22. = CONTRIBUTION A LA PATHOLOGIE DU CHROMOSOME 22GIORDANO A; GRIMOLDI MG; LAVEZZI AM et al.1976; FOLIA HERED. PATHOL.; ITAL.; DA. 1976; VOL. 25; NO 2; PP. 38-52; ABS. ANGL.; BIBL. 1 P. 1/2Article

DUPLICATION OF THE SEGMENT Q122->QTER OF CHROMOSOME 22 DUE TO PATERNAL INVERSION 22 (P13Q122)FUJIMOTO A; WILSON MG; TOWNER JW et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 82-84; BIBL. 3 REF.Article

PHENOTYPIC VARIATION IN TWO PATIENTS WITH A RING CHROMOSOME 22FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 5; PP. 305-310; BIBL. 23 REF.Article

The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesISELIUS, L; LINDSTEN, J; DUTRILLAUX, B et al.Human genetics. 1983, Vol 64, Num 4, pp 343-355, issn 0340-6717Article

Report of the third international workshop on human chromosome 22 mappingEMANUEL, B. S; BUETOW, K; NUSSBAUM, R et al.Cytogenetics and cell genetics. 1993, Vol 63, Num 4, pp 206-211, issn 0301-0171Article

Chiasma-derived genetic lengths and recombination fractions: a reciprocal translocation 46,XY,t(1; 22)(q32; q13)PALMER, R. W; HULTEN, M. A.Annals of human genetics. 1983, Vol 47, Num 4, pp 299-310, issn 0003-4800Article

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