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A(6; 18) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-610KLINGER HP; ARONSON MM; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 402-403; BIBL. 1 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

AUTOSOMAL IMBALANCE WITH A NEAR-NORMAL PHENOTYPE: THE SMALL EFFECT OF TRISOMY FOR THE SHORT ARM OF CHROMOSOME 18GARDNER RJM; RUDD NL; STEVENS LJ et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 359-363; BIBL. 2 REF.Article

PARTIAL TRISOMY OF CHROMOSOME 18 (PTER->Q 11) A DISCUSSION ON THE IDENTIFICATION OF THE CRITICAL SEGMENTSAN MARTIN V; FERNANDEZ NOVOA C; HEVIA A et al.1981; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1981; VOL. 24; NO 4; PP. 248-250; ABS. FRE; BIBL. 9 REF.Article

TRANSLOCATIONS TERMINO-TERMINALES DE NOVO ENTRE DEUX CHROMOSOMES 18: A PROPOS DE DEUX OBSERVATIONS 46, XY, TER REA (18; 18) (PTER; PTER)LAURENT C; BIEMONT MC; PHILIP T et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 78-82; ABS. ENG; BIBL. 15 REF.Article

THE TRISOMY 18 SYNDROME WITH AN E/G TRANSLOCATIONDZIEKANOWSKA D; DZIUBA P; SOBANSKI T et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 347-349; BIBL. 7 REF.Article

MEIOTIC CHROMOSOME STUDY IN A HUMAN FEMALE TRANSLOCATION HETEROZYGOTE = ETUDE DES CHROMOSOMES EN MEIOSE CHEZ UNE FEMME PORTEUSE D'UNE TRANSLOCATION HETEROZYGOTEUEBELE KALLHARDT B; KNOERR K.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 4; PP. 355-356; BIBL. 3 REF.Article

DAS 18Q--SYNDROM = LE SYNDROME 18Q-SCHINZEL A; HAYASHI K; SCHMID W et al.1975; ARCH. GENET.; SCHWEIZ; DA. 1975; VOL. 48; NO 1; PP. 76; (SCHWEIZ. GES. GENET. JAHRESVERSAMML. ZUSAMMENFASSUNGEN REFRATE; LAUSANNE; 1974)Conference Paper

FAMILIAL MENTAL RETARDATION IN A FAMILY WITH AN INHERITED CHROMOSOME REARRANGEMENT = ARRIERATION MENTALE FAMILIALE DANS UNE FAMILLE CONDUCTRICE D'UN REMANIEMENT CHROMOSOMIQUE HEREDITAIRECHUDLEY AE; BAUDER F; RAY M et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 353-366; BIBL. 40REF.Article

FAMILIAL PARTIAL DISTAL 18Q (18Q22-18Q23) TRISOMYDE MUELENAERE A; FRYNS JP; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 184-186; ABS. FRE; BIBL. 4 REF.Article

A CASE OF PARTIAL 3P TRISOMY (46,XY,-18,+DER(18),T(3; 18) (P24; Q22))TSUKINO R; OMORI H; UEMURA S et al.1981; PROC. JPN. ACAD., SER. B; ISSN 0386-2208; JPN; DA. 1981; VOL. 57; NO 3; PP. 89-94; BIBL. 8 REF.Article

TRISOMY 18 Q-. TRISOMY MAPPING OF CHROMOSOME 18 REVISITEDTURLEAU C; CHAVIN COLIN F; NARBOUTON R et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 1; PP. 20-26; BIBL. 11 REF.Article

TRISOMY 18QTER AND TRISOMY MAPPING OF CHROMOSOME 18.TURLEAU C; DE GROUCHY J.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 6; PP. 361-371; BIBL. 18 REF.Article

CONTRIBUTION A L'ETUDE DU CHROMOSOME 18 EN ANNEAU (A PROPOS DE DEUX OBSERVATIONS).WALLERICH THEOBALD MF.1977; ; S.L.; DA. 1977; PP. 1-82; BIBL. 25 P.; (THESE DOCT. MED.; NANCY I)Thesis

A CASE OF RING 18 CHROMOSOME IN A SIBSHIP WITH MULTIPLE SPONTANEOUS ABORTIONSCOCO R; BARREIRO CZ; PENCHASZADEH VB et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 135-137; ABS. FR.; BIBL. 3REF.Article

TETRASOMY 18 P: TENTATIVE DELINEATION OF A SYNDROMEBATISTA DAS; VIANNA MORGANTE AM; RICHIERI COSTA A et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 144-147; BIBL. 10 REF.Article

KARYOTYPE 47, XXY, 18P IN A NEWBORN CHILD WITH HOLOPROSENCEPHALYSCHNABEL R; HANSEN S.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 3; PP. 186-190; BIBL. 16 REF.Article

RING 18 MOSAICISM IN IDENTICAL TWINSHATA A; SUZUKI Y; MATSUI I et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 364-367; BIBL. 11 REF.Article

ANOMALIES CONSTITUTIONNELLES DU CHROMOSOME 18: MONOSOMIES PARTIELLES, ANNEAUX, TRISOMIE COMPLETE LIBRE. ETUDE DE CAS PERSONNELS ET REVUE DE LA LITTERATUREBRES MICHEL.1979; ; FRA; DA. 1979; 24; 88 P.: ILL.-PL.; 30 CM; BIBL. 61 REF.; TH.: MED./TOURS/1979Thesis

TRISOME PARTIELLE 7Q. UN OU DEUX SYNDROMES. A PROPOS D'UNE NOUVELLE OBSERVATIONTURLEAU C; ROSSIER A; DE MONTIS G et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 37-42; ABS. ANGL.; BIBL. 13 REF.Article

UN CAS DE TRANSLOCATION D/E:45XX,13-,18-,T(18Q+,13-)BUDYAKOV VI; BONDARENKO ES; ZUBKOVA VL et al.1975; GENETIK; S.S.S.R.; DA. 1975; VOL. 11; NO 3; PP. 133-137; ABS. ANGL.; BIBL. 23 REF.Article

DE NOVO PARTIAL TRISOMY OF CHROMOSOME 18 (PTER->911:): SOME OBSERVATIONS ON THE PHENOTYPE MAPPING OF CHROMOSOME 18 IMBALANCESHERNANDEZ A; CORONA RIVERA E; PLASCENCIA L et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 165-167; ABS. FRE; BIBL. 6 REF.Article

FEATURES OF TRISOMY 18 AND 18P-SYNDROMES IN AN INFANT WITH 46, XY, I (18Q)BASS HN; SPARKES RS; MILLER AA et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 163-168; BIBL. 5 REF.Article

TRISOMY 18 SYNDROME WITH AN UNUSUAL KARYOTYPE: POSSIBLE DOUBLE ISOCHROMOSOME.LARSON LM; WASDAHL WA; SAUMUR JH et al.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 1; PP. 73-76; BIBL. 11 REF.Article

NUMERISCHE UND STRUKTURELLE ABERRATIONEN DES CHROMOSOMS NR. 18. = LES ABERRATIONS NUMERIQUES ET STRUCTURELLES DU CHROMOSOME NO 18AKSU F; MIETENS C; SCHOLZ W et al.1976; KLIN. PAEDIATR.; DTSCH.; DA. 1976; VOL. 188; NO 3; PP. 220-232; ABS. ANGL.; BIBL. 2 P. 1/2Article

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