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kw.\*:("ABNORMAL G22 CHROMOSOME")

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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

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

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

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

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

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

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

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

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

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

ANOMALIE CHROMOSOMIQUE NOUVELLE PAR TRANSLOCATION T (20;22) AU COURS D'UNE LEUCEMIE MYELOIDE CHRONIQUELAI JL; JOUET JP; BAUTERS F et al.1982; NOUVELLE PRESSE MEDICALE; ISSN 0301-1518; FRA; DA. 1982; VOL. 11; NO 44; PP. 3270; BIBL. 3 REF.Article

UNUSUAL TRANSLOCATION AND CHRONIC MYELOCYTIC LEUKEMIA: "MASKED" PHILADELPHIA CHROMOSOME (PH1)LESSARD M; DUVAL S; FRITZ A et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 3; PP. 237-244; BIBL. 15 REF.Article

PARTIAL TRISOMY 22Q WITH ELEVATED ARYLSULFATASE-A ACTIVITYFRYNS JP; JAEKEN J; VAN DEN BERGHE H et al.1979; AM. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 169-170; ABS. FRE; BIBL. 9 REF.Article

ONE CASE OF A PH CHROMOSOME RESULTING FROM TRANSLOCATION OF THE DISTAL END OF 22Q ONTO THE SHORT ARM OF CHROMOSOME 15.JOTTERAND BELLOMO M.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 21; NO 3; PP. 168-169; BIBL. 2 REF.Article

PARTIAL TRISOMY 22: A RECOGNIZABLE SYNDROME.GARLINGER P; MCGEARY SA; MAGENIS E et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 1; PP. 9-16; BIBL. 19 REF.Article

RECURRENT ABORTION ASSOCIATED WITH A BALANCED 22;22 TRANSLOCATION, OR ISOCHROMOSOME 22Q IN A MONOZYGOUS TWIN.LEWIS BV; RIDLER MAC.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 1; PP. 81-85; BIBL. 9 REF.Article

LA TRISOMIE 9P. UN CAS DE TRANSLOCATION T(9;22) (P11;P11)-MAT CHEZ UNE FILLETTE.GENEST P; ROUSSY J; GENEST FB et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 7; PP. 956-959; ABS. ANGL.; BIBL. 14 REF.Article

TRANSLOCATION FAMILALE 3/22 MAT AVEC TRISOMIE PARTIELLE 3Q.SCHWANITZ G; SCHMID RD; GROSSE G et al.1977; J. GENET. HUM.; SUISSE; DA. 1977; VOL. 25; NO 2; PP. 141-150; ABS. ANGL. ALLEM.; BIBL. 4 REF.Article

A CASE OF CHRONIC MYELOID LEUKEMIA WITH A TRANSLOCATION (12;22) (P13;G11).VAN DER BLIJ PHILIPSEN M; BREED WPM; HUSTINX TWJ et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 229-231; BIBL. 13 REF.Article

A NEX TRANSLOCATION INVOLVING THREE CHROMOSOMES IN CHRONIC MYELOCYTIC LEUKEMIA, 46, XY, T(9;11;22).GAHRTON G; FRIBERG K; ZECH L et al.1977; CYTOGENET. CELL GENET.; SWITZ; DA. 1977; VOL. 18; NO 2; PP. 75-81; BIBL. 1 P. 1/2Article

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