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CLINICAL FEATURES OF MONOSOMY 10QTERZATTERALE A; PAGANO L; FIORETTI G et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 106-108; ABS. FRE; BIBL. 17 REF.Article

TERMINAL DELECTION OF THE LONG ARM OF CHROMOSOME 10: Q26->QTER: CASE REPORT AND REVIEW OF LITERATURETAYSI K; STRAUSS AW; YANG V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 141-144; ABS. FRE; BIBL. 3 REF.Article

RING CHROMOSOME 10: 46, XX, R (10) (P15->Q26)TSUKINO R; TSUDA N; DEZAWA T et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 2; PP. 148-151; BIBL. 4 REF.Article

A (10;17) TRANSLOCATION, UNBALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-217ZACKAL E; MELLMAN W; ARONSON M et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 90-91; BIBL. 1 REF.Article

A CASE OF 10P- SYNDROMESUCIU S; NANULESCU M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 109-111; ABS. FRE; BIBL. 11 REF.Article

PHENOTYPE ASSOCIATED WITH RING 10 CHROMOSOME: REPORT OF PATIENT AND REVIEW OF LITERATUREMICHELS VV; DRISCOLL DJ; LEDBETTER DH et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 231-237; BIBL. 11 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

LA TRISOMIE 10Q24->10QTERPRIEUR M; FORABOSCO A; DUTRILLAUX B et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 217-222; ABS. ANGL.; BIBL. 14 REF.Article

A (7; 10) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-44MILLER RC; BRADT C; NICHOLS WW et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 86-87Article

DUPLICATION DEFICIENCY AS THE RESULT OF MEIOTIC SEGREGATION OF A MATERNAL INV (10)YUNIS E; TORRES DE CABALLERO O.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 71-74; BIBL. 23 REF.Article

SERIAL DUPLICATION OF 10(Q21->Q22) IN A MENTALLY RETARDED BOY WITH CONGENITAL MALFORMATIONSKOIVISTO M; HERVA R; LINNA SL et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 224-225; BIBL. 6 REF.Article

RING CHROMOSOME 10 ASSOCIATED WITH MULTIPLE CONGENITAL MALFORMATIONSSIMONI G; ROSSELLA F; DALPRA L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 117-121; BIBL. 8 REF.Article

A (10; 17) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-216ZACKAL E; MELLMAN W; ARONSON M et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 88-89; BIBL. 1REF.Article

A 46,XX,10Q+ CHROMOSOME CONSTITUTION IN A GIRL. PARTIAL LONG ARM DUPLICATION OR INSERTIONAL TRANSLOCATION. = CONSTITUTION CHROMOSOMIQUE 46,XX,10Q+ CHEZ UNE FILLE. DUPLICATION PARTIELLE DU BRAS LONG OU TRANSLOCATION AVEC INSERTION.ORYE E; VERHAAREN H; SAMUEL K et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 1; PP. 1-8; BIBL. 8 REF.Article

PARTIAL TRISOMY 10Q IN THREE UNRELATED PATIENTSTAYSI K; YANG V; MONAGHAN N et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 79-85; ABS. FRE; BIBL. 10 REF.Article

TRISOMY OF THE DISTAL THIRD OF THE LONG ARM OF CHROMOSOME 10. REPORT OF A NEW CASE DUE TO A FAMILIAL TRANSLOCATION T (10;18) (Q 24; P 11). = UNE TRISOMIE DU TIERS DISTAL DU BRAS LONG DU CHROMOSOME 10. RAPPORT D'UN NOUVEAU CAS DU A UNE TRANSLOCATION FAMILIALE T (10; 18) (Q 24; P 11)FORABOSCO A; BERNASCONI S; GIOVANNELLI G et al.1975; HELV. PAEDIATR. ACTA; SUISSE; DA. 1975; VOL. 30; NO 3; PP. 289-295; ABS. ALLEM. FR.; BIBL. 9 REF.Article

IS THERE A MONOSOMY 10 QTER SYNDROME.MULCAHY MT; PEMBERTON PJ; THOMPSON E et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 1; PP. 33-35; BIBL. 3 REF.Article

MECANISMES DE FORMATION DES DUPLICATIONS: A PROPOS D'UNE OBSERVATION DE DUPLICATION 10Q22->Q25PISON H; SELE B; SALVAT J et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 137-140; ABS. ENG; BIBL. 16 REF.Article

DISTAL 10P DELETION SYNDROMEFRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 189-190; ABS. FRE; BIBL. 7 REF.Article

BALANCED TRANSMISSION OF CENTROMERIC FISSION PRODUCTS IN MANFRYNS JP; BULCKE J; HENS L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 127-128; BIBL. 7 REF.Article

RING 10 CHROMOSOME: 46, XX, R10 (P15 Q26)SPARKES RS; LING SM; MULLER H et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 341-345; BIBL. 16 REF.Article

DELETION-TRANSLOCATION DEL(12)(P11)->T(10;12)(P13;P11)NIELSEN J; RASMUSSEN K; NIEBUHR E et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 53-55; ABS. FR.; BIBL. 36 REF.Article

TRISOMIE 10P. UNE OBSERVATION ANCIENNE PRECISEE PAR MARQUAGETURLEAU C; DE BAZIGNAN MD; ROUBIN M et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 61-64; ABS. ANGL.; BIBL. 6 REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME 10NAKAGOME Y; KOBAYASHI H.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 412-414; BIBL. 4 REF.Article

RING CHROMOSOME 10 AND ITS CLINICAL FEATURESNAKAI H; ADACHI M; KATSUSHIMA N et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 142-144; BIBL. 5 REF.Article

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