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FREQUENCY AND SEGREGATION OF 16 QH+ = FREQUENCE ET SEGREGATION DE 16 QH+NIELSEN J; FRIEDRICH U; HREIDARSSON AB et al.1974; CLIN. GENET.; DANM.; DA. 1974; VOL. 5; NO 4; PP. 316-321; BIBL. 9REF.Article

NEW CHROMOSOME POLYMORPHISM: INV(16)(P11Q12OR13).FONATSCH C.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 2; PP. 106-107; BIBL. 5 REF.Article

PSEUDOHERMAPHRODITISM WITH CLINICAL FEATURES OF TRISOMY 18 IN AN INFANT TRISOMIC FOR PARTS OF CHROMOSOMES 16 AND 18: 47, XY, DER(18), T(16; 18) (P12; Q11) MAT.STERN LM; MURCH AR.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 3; PP. 305-307; BIBL. 6 REF.Article

HOMODICENTRIC CHROMOSOMES: A DISTINCTIVE TYPE OF DICENTRIC CHROMOSOMEWARD BE; BRADLEY CM; COOPER JB et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 54-58; BIBL. 15 REF.Article

INTERSTITIAL 16Q DELETION WITH TYPICAL DYSMORPHIC SYNDROMEFRYNS JP; PROESMANS W; VAN HOEY G et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 2; PP. 124-125; ABS. FRE; BIBL. 4 REF.Article

PARTIAL MONOSOMY OF THE LONG ARM OF CHROMOSOME 16 IN A MALFORMED NEWBORN: KARYOTYPE 46, XX, DEL (16) (Q21).FRYNS JP; MELCHOIR S; JAEKEN J et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 3; PP. 343-346; BIBL. 3 REF.Article

ABNORMALITY OF CHROMOSOME 16 AND ITS PHENOTYPIC EXPRESSIONGOLDEN NL; BILENKER R; JOHNSON WE et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 1; PP. 41-45; BIBL. 8 REF.Article

DE NOVO TRISOMY 1611->PTERDALLAPICCOLA B; CURATOLO P; BALESTRAZZI P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 1; PP. 1-6; BIBL. 6 REF.Article

A TERMINAL LONG ARM DELETION OF CHROMOSOME 16 IN A DYSMORPHIC INFANT: 46, XY, DEL (16) (Q22)TAYSI K; FISHMAN M; SEKHON GS et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 343-347; BIBL. 4 REF.Article

THE FRAGILE SITE ON CHROMOSOME 16 (Q21Q22): DATA ON FOUR NEW FAMILIESSHABTAI F; BICHACHO S; HALBRECHT I et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 19-22; BIBL. 14 REF.Article

DUPLICATION OF 16P FROM INSERTION OF 16P INTO 16Q WITH SUBSEQUENT DUPLICATION DUE TO CROSSING OVER WITHIN THE INSERTED SEGMENTCOHEN MM; LERNER C; BALKIN NE et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 89-96; BIBL. 9 REF.Article

RING CHROMOSOME 16NEIDENGARD L; SPARKES RS.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 175-177; BIBL. 11 REF.Article

ERYNS SYNDROME WITHOUT DELETION 16 QCOTE GB; PAPADAKOU LAGOYANNI S; KAIRIS M et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 171-172; ABS. FRE; BIBL. 5 REF.Article

AN ATTEMPT TO DEFINE 1QH+, 9PH+, AND 16QH+FRIEDRICH U; THERKELSEN AJ.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 139-144; BIBL. 9 REF.Article

FIVE FAMILIAL CASES WITH A TRISOMY 16 P SYNDROME DUE TO TRANSLOCATIONLESCHOT NJ; DE NEF JJ; GERAEDIS JPM et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 205-214; BIBL. 5 REF.Article

HEMOGLOBIN H DISEASE AND MENTAL RETARDATION: A NEW SYNDROME OR A REMARKABLE COINCIDENCE.WEATHERALL DJ; HIGGS DR; BUNCH C et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 305; NO 11; PP. 607-612; BIBL. 20 REF.Article

MONOSOMY 10 QTER DUE TO A BALANCED FAMILIAL TRANSLOCATION: T(10; 16) (Q 25.2; Q24)WEGNER RD; KUNZE J; PAUST H et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 2; PP. 130-133; BIBL. 5 REF.Article

PARTIAL TRISOMY FOR LONG ARM OF CHROMOSOME 16BUCKTON KE; BARR DGD.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 6; PP. 483; BIBL. 3 REF.Article

BALANCED RECIPROCAL TRANSLOCATION T(1;16) (Q12;Q11) IN TWO GENERATIONS OF A FAMILYESSER KJ; HABEDANK M.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 1; PP. 92; BIBL. 2 REF.Article

A CULTURE WITH A DERIVATIVE CHROMOSOME 10 FROM A PATERNAL (10;16) TRANSLOCATION. REPOSITORY IDENTIFICATION NO 6M-139B.EMANUEL B; ZACKAI EH; HELLMAN WJ et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 4; PP. 240Article

HETEROCHROMATIC REGIONS ON CHROMOSOMES 1,9, 16, AND Y IN CHILDREN WITH SOME DISTURBANCES OCCURING DURING EMBRYO DEVELOPMENTPODUGOLNIKOVA OA; BLUMINA MG.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 2; PP. 183-188; BIBL. 28 REF.Article

ANTIKOERPERMANGELSYNDROM UND CHROMOSOMENANOMALIEN. = SYNDROME DE DEFICIT EN ANTICORPS ET ANOMALIES CHROMOSOMIQUESWIERSBITZKY S; SCHROETER C.1976; ALLERGIE U. IMMUNOL.; DTSCH.; DA. 1976; VOL. 22; NO 2; PP. 167-170; ABS. ANGL.; BIBL. 28 REF.Article

AUGMENTATION D'ACTIVITE DE L'ADENINE PHOSPHORIBOSYL TRANSFERASE CHEZ UN ENFANT TRISOMIQUE 16Q22.2->16PTER PAR TRANSLOCATION T(16;21) (Q22.2;Q22.2) PATRETHORE MO; LAFOURCADE J; COUTURIER J et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 36-42; ABS. ENG; BIBL. 27 REF.Article

A CASE OF INVERTED INSERTION ASSESSED BY R AND G BANDINGDE ARCE MA; LAW E; MARTIN L et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 148-151; BIBL. 5 REF.Article

TRISOMY 209 DUE TO MATERNAL T(16; 20) TRANSLOCATION. FIRST CASEPAWLOWITZKI IH; GROBE H; HOLZGREVE W et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 2; PP. 167-170; BIBL. 7 REF.Article

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