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A SUBTELOCENTRIC CHROMOSOME 9 IN A DYSPLASTIC 18-YEAR-OLD BOY WITH DISSOCIATED MENTAL DEVELOPMENT = CHROMOSOME 9 SUBTELOCENTRIQUE CHEZ UN GARCON DE 18 ANS DYSPLASIQUE AU DEVELOPPEMENT MENTAL DISSOCIEHANSMANN I; KEUTEL J.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 4; PP. 287-289; BIBL. 10 REF.Article

INVERSION HOMOZYGOSITY OF CHROMOSOME NO.9 IN A HIGHLY INBRED KINDREDVINE DT; YARKONI S; COHEN MM et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 3; PP. 203-207; BIBL. 9 REF.Article

ON THE MONOCLONAL ORIGIN OF CHRONIC MYELOCYTIC LEUKEMIA. = SUR L'ORIGINE MONODONALE DE LA LEUCEMIE MYELOCYTAIRE CHRONIQUEHAYATA I; KAKATI S; SANDBERG AA et al.1974; PROC. JAP. ACAD.; JAP.; DA. 1974; VOL. 50; NO 5-6; PP. 381-385; BIBL. 10 REF.Article

ASSOCIATION OF PERICENTRIC INVERSION OF CHROMOSOME 9 AND REPRODUCTIVE FAILURE IN TEN UNRELATED FAMILIESBOUE J; TAILLEMITE JL; HAZAEL MASSIEUX P et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 217-224; BIBL. 1 P.Article

L'INSTABILITE PSYCHO-MOTRICE EST-ELLE VRAIMENT UN SIGNE CARACTERISTIQUE DE LA TRISOMIE 9P.: A PROPOS DE 3 OBSERVATIONSLE MAREC B; BOUCHARD C; BOIXEL J et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 263-269; ABS. ENG; BIBL. 8 REF.Article

CHROMOSOMAL VARIANTS AND NONDISJUNCTION.FORD JH; LESTER P.1978; CYTOGENET. CELL. GENET.; CHE; DA. 1978; VOL. 21; NO 5; PP. 300-303; BIBL. 10 REF.Article

UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTINOI MF; VAN DEN AKKER J; LE PORRIER N et al.1983; SEMAINE DES HOPITAUX; ISSN 0037-1777; FRA; DA. 1983; VOL. 59; NO 3; PP. 185-188; ABS. ENG; BIBL. 12 REF.Article

9P TRISOMY IDENTIFIED BY GIEMSA-11WYANDT HE; HECHT F; MAGENIS RE et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 355-358; BIBL. 8 REF.Article

PERICENTRIC INVERSIONS OF HUMAN CHROMOSOMES 9 AND 10 = INVERSIONS PERICENTRIQUES DES CHROMOSOMES HUMAINS 9 ET 10DE LA CHAPELLE A; SCHROEDER J; STENSTRAND K et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 26; NO 6; PP. 746-766; BIBL. 2P.Article

UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTNOL MF; VAN DEN AKKER J; LE PORRIER N et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 164-167; ABS. ENG; BIBL. 12 REF.Article

47, XY, T(9P+; 11Q+) IN A MALE INFANT WITH MULTIPLE MALFORMATIONS = , XY, T (9P+; 11Q+) CHEZ UN NOURRISSON MALE POLYMALFORMEDINNO ND; SILVEY GL; WEISSKOPF B et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 125-131; BIBL. 11REF.Article

A RING 9 CHROMOSOME. REPOSITORY IDENTIFICATION NO. GM-166KISTENMACHER ML; PUNNETT HH; ARONSON M et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 2; PP. 122-123; BIBL. 1 REF.Article

MODERATE MENTAL RETARDATION AND NONSPECIFIC DYSMORPHIC SYNDROME ASSOCIATED WITH RING CHROMOSOME 9FRYNS JP; LAMBRECHTS A; JANSSEUNE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 29-32; BIBL. 15 REF.Article

MENTAL RETARDATION AND CONGENITAL MALFORMATIONS ASSOCIATED WITH A RING CHROMOSOME 9NAKAJIMA S; YANAGISAWA M; KAMOSHITA S et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 3; PP. 289-293; BIBL. 13 REF.Article

Tetrasomy 9p confirmed by GALTBALESTRAZZI, P; CROCI, G; FRASSI, C et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 396-399, issn 0022-2593Article

DUPLICATION OF THE SHORT ARM OF CHROMOSOME 9. ANALYSIS OF FIVE CASESCUOCO C; GIMELLI G; PASQUALI F et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 3-7; BIBL. 22 REF.Article

CYTOGENETIQUE D'UN PATIENT PORTEUR DE DELETION DES CONSTRICTIONS SECONDAIRES DU CHROMOSOME 9 ET ETUDE FAMILIALEHE XIAOXUAN; XIA JIAHUI; LI LUYUN et al.1982; YICHUAN XUEBAO. (ACTA GENETICA SINICA); ISSN 0379-4172; CHN; DA. 1982; VOL. 9; NO 4; PP. 315-319; ABS. ENG; BIBL. 12 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 9. A CLINICALLY RECOGNISABLE ENTITYFRYNS JP; PEDERSEN JC; DUYCK H et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 3; PP. 201-204; BIBL. 15 REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME NUMBER 9: A CLINICAL ENTITYFRYNS JP; VAN DEN BERGHE H.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; SUPPL.; 8 P.; BIBL. 5 REF.Article

PERICENTRIC INVERSIONS OF CHROMOSOME NUMBER 9: BENIGN OR HARMFUL.HOWARD PEEBLES PN; STODDARD GR.1979; HUM. HERED.; CHE; DA. 1979; VOL. 29; NO 2; PP. 111-117; BIBL. 2 P.Article

THE DERMATOGLYPHIC PATTERN OF THE TRISOMY 9P SYNDROMERODEWALD A; STENGEL RUTKOWSKI S; ZANKL M et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 6; PP. 405-417; BIBL. 2 P.Article

TRISOMY 9P WITH AN ISOCHROMOSOME OF 9PSMITH G; MCCAA A; KELLY TE et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 125-126; BIBL. 15 REF.Article

PRESENCE, CHEZ UN HOMME STERILE, DE DEUX INVERSIONS PERICENTRIQUES DES CHROMOSOMES 9: INV(9) (P11Q1209), INV(9) (PTER1209)CROQUETTE MF; COUTURIER J; DUTRILLAUX B et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 1; PP. 53-56; ABS. ENG; BIBL. 11 REF.Article

LANG. ENGPAULI RM; PAGON RA; HALL JG et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 297-301; BIBL. 25 REF.Article

PARTIAL TETRASOMY 9 IN A LIVEBORN INFANTWISNIEWSKI L; POLITIS GD; HIGGINS JV et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 147-153; BIBL. 8 REF.Article

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