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A NOTE ON A PATIENT WITH A RING-22 CHROMOSOME IDENTIFIED BY BANDINGSTEWART A; RICHARDS BW.1976; J. MENTAL DEFIC. RES.; G.B.; DA. 1976; VOL. 20; NO 2; PP. 95-98; BIBL. 2 REF.Article

A(13; 22) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-627KIM HJ; HIRSCHHORN K; HSU LYF et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 406-407Article

PHILADELPHIA CHROMOSOME WITH T(6;22) (P25;Q12)MAMMON Z; GRINBLAT J; JOSHUA H et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 16; PP. 827-828; BIBL. 8 REF.Article

A POSSIBLE CASE OF PARTIAL TRISOMY FOR CHROMOSOME 22: FURTHER EVIDENCE FROM GIEMSA BANDING STUDIES = UN CAS POSSIBLE DE TRISOMIE PARTIELLE DU CHROMOSOME 22: NOUVEAUX ARGUMENTS D'APRES L'ETUDE DES COLORATIONS EN BANDE PAR LE GIEMSASANDS ME.1974; J. MENTAL DEFIC. RES.; G.B.; DA. 1974; VOL. 18; NO 4; PP. 327-330; BIBL. 2 REF.Article

A (17; 22) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-119MACINTYRE MN; HEMPEL JM; WALDEN DB et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 80-81; BIBL. 2REF.Article

A (13;22) ROBERTSONIAN TRANSLOCATION, 45 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-392ALFI O; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 1; PP. 55-56Article

THREE GENERATIONS AND SEVEN FAMILY MEMBERS WITH A T(21Q22Q) CHROMOSOME = CHROMOSOME T(21Q22Q) CHEZ SEPT MEMBRES D'UNE FAMILLE SUR TROIS GENERATIONSZERGOLLERN L.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 379-381; BIBL. 5REF.Article

FAMILIAL 21/22 TRANSLOCATIONPAPP Z; DOLHAY B; GARDO S et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 69-73; ABS. ITAL. FR. ALLEM.; BIBL. 18 REF.Article

SEGREGATION OF A T(14Q22Q) CHROMOSOME IN A LARGE KINDRED = SEGREGATION D'UN CHROMOSOME T(14Q22Q) DANS UNE GRANDE FAMILLENEU RL; VALENTINE FA; GARDNER LI et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 30-36; BIBL. 14 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

UNEXPECTED FINDINGS WITH THE NEW CHROMOSOME BANDING TECHNIQUES IN A PATIENT FORMERLY DIAGNOSED AS HAVING G-DELETION SYNDROME = RESULTATS INATTENDUS OBTENUS GRACE AUX NOUVELLES TECHNIQUES DE BANDES CHEZ UNE PATIENTE DIAGNOSTIQUEE INITIALEMENT COMME ATTEINTE DE SYNDROME II DE DELETION GORYE E; CRAEN M.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 75-82; ABS. ITAL. FR. ALLEM.; BIBL. 14 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

A NEW TRANSLOCATION IN CHRONIC MYELOGENOUS LEUKEMIAPRAVTCHEVA D; ANDREEVA P; TSANEVA R et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 229-232; BIBL. 11 REF.Article

TRANSMISSION OF A T(13Q22Q) CHROMOSOME ABSERVED IN THREE GENERATIONS WITH SEGREGATION OF THE TRANSLOCATION D1-TRISOMY SYNDROMEABE T; MORITA M; KAWAI K et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 207-215; BIBL. 21 REF.Article

DEUX CAS DE TRISOMIE 11Q (Q231-QTER) PAR TRANSLOCATION T(11,22) (Q231; Q111) DANS DEUX FAMILLES DIFFERENTES.AURIAS A; TURC C; MICHIELS Y et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 185-188; ABS. ANGL.; BIBL. 9 REF.Article

TRISOMIE 9P PAR TRANSLOCATION MATERNELLE (9;22)(P11;Q11)PHILIPPE N; REQUIN C; GERMAIN D et al.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 4; PP. 309-317; ABS. ANGL. ALLEM.; BIBL. 1 P. 1/2Article

HUMAN INHERITED MARKER CHROMOSOME 22 SHORT-ARM ENLARGEMENT: INVESTIGATION OF RDNA GENE MULTIPLICITY, AG-BAND SIZE, AND ACROCENTRIC ASSOCIATIONBERNSTEIN R; DAWSON B; GRIFFITH J et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 135-139; BIBL. 22 REF.Article

PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 22 (22 Q 13) WITH COMPLETE 22 TRISOMY PHENOTYPEFRYNS JP; DE BACKER D; LEMLI L et al.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; NO 2; PP. 125-127; BIBL. 8 REF.Article

A FURTHER CASE OF A 22; 22 ROBERTSONIAN TRANSLOCATION ASSOCIATED WITH RECURRENT ABORTIONS.MAMELI M; CARDIA S; MILIA A et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 359-361; BIBL. 5 REF.Article

PHENOTYPIC CORRELATIONS IN PATIENTS WITH RING CHROMOSOME 22.HUNTER AGW; RAY M; WANG HS et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 4; PP. 239-249; BIBL. 26 REF.Article

VARIABILITY OF R(22) CHROMOSOME PHENOTYPICAL EXPRESSION.DALLAPICCOLA B; BRINCHI V; CURATOLO P et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 287-290; BIBL. 4 REF.Article

A CASE OF RING CHROMOSOME G22.BROOKFIELD DSK; WALKER S.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 530-532; BIBL. 6 REF.Article

A22/22 TRANSLOCATION CARRIER WITH RECURRENT ABORTIONS DEMONSTRATED BY A GIEMSA BANDING TECHNIQUEMAEDA T; OHNO M; SHIMADA N et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 2; PP. 243-245; BIBL. 11 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

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