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PAETAU-SYNDROM: TRISOMIE 13 = SYNDROME DE PATAU: TRISOMIE 13HEUFT G; FINK M; BOEHM N et al.1980; MED. WELT; DEU; DA. 1980; VOL. 31; NO 15; PP. 545-549; BIBL. 46 REF.Article

PROBABLE AUTOSOMAL RECESSIVE MARFAN SYNDROME.FRIED K; KRAKOWSKY D.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 5; PP. 359-361; BIBL. 3 REF.Article

A LETHAL, LARSEN-LIKE MULTIPLE JOINT DISLOCATION SYNDROMECHEN H; CHUNG HO CHANG; PERRIN E et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 2; PP. 149-161; BIBL. 2 P.Article

INHERITANCE OF TIBIAL HEMIMELIA IN GALLOWAY CATTLE.LEIPOLP HW; SAPERSTEIN G; SWANSON R et al.1978; Z. TIERZUECHT. ZUECHT.-BIOL.; DTSCH.; DA. 1978; VOL. 94; NO 3-4; PP. 291-295; ABS. ESP. ALLEM.; BIBL. 6 REF.Article

PSEUDOPROGERIA/HALLERMANN-STREIFF (PHS) SYNDROME.HALL BD; BERG BO; RUDOLPH RS et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 137-146; BIBL. 6 REF.Article

A LINEBIRTH WITH TRIPLOIDY SYNDROME (69, XXX)RUSSELL MH; SHENAI JP; NIBLACK GD et al.1981; CLIN. PEDIATR.; ISSN 0009-9228; USA; DA. 1981; VOL. 20; NO 12; PP. 806-807; BIBL. 9 REF.Article

AUTOSOMAL DOMINANT FIRST AND SECOND BRANCHIAL ARCH SYNDROME. A NEW INHERITED SYNDROME.KARMODY CS; FEINGOLD M.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 31-40; BIBL. 11 REF.Article

MALFORMATION SYNDROMES.1976; BRITH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1976; VOL. 12; NO 5; PP. 181-333; BIBL. DISSEM.; (CYTOGENET. ENVIRON. MALFORM. SYNDROMES. CONF.; KANSAS CITY, MO.; 1975)Conference Paper

THE HUMAN SIMIAN CREASE AND ITS VARIANTS. A MODEL FOR INVESTIGATION OF SERIOUS CONGENITAL MALFORMATION.HOOK EB; BONENFANT R; POWERS ML et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 7-16; BIBL. 14 REF.Article

HYDROMETROCOLPOS-POLYDACTYLY SYNDROME IN A MACERATED FEMALE FOETUSHASPESLAGH M; FRYNS JP; VAN DER BERGHE K et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 136; NO 3; PP. 307-309; BIBL. 11 REF.Article

INTERET DU DIAGNOSTIC RETROSPECTIF D'UN SYNDROME MALFORMATIF LETHAL (A PROPOS D'UNE TRISOMIE 18)COUSIN J; CROQUETTE MF; CREUSY GUILBERT C et al.1979; J. SCI. MED. LILLE; FRA; DA. 1979; VOL. 97; NO 2; PP. 59-60Article

A LOW FREQUENCY MOSAICISM FOR MONOSOMY 21 IN A LIVE BORN FEMALEMING LIANG LEE; ROSE D; LAZZARINI A et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 3; PP. 343-347; BIBL. 8 REF.Article

CYTOGENETIC STUDY OF INDIVIDUALS SUSPECTED OF CHROMOSOME ANOMALIES.SINGH DN.1977; CLIN. PEDIATR.; U.S.A.; DA. 1977; VOL. 16; NO 7; PP. 619-622; BIBL. 13 REF.Article

NUMERICAL TAXONOMY IN CLINICAL GENETICS.HERRMANN J.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3A; PP. 39-52; BIBL. 5 REF.Article

ANOPHTHALMOS IN AN INFANT WITH MULTIPLE CONGENITAL ANOMALIES.SASSANI JW; YANOFF M.1977; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1977; VOL. 83; NO 1; PP. 43-48; BIBL. 26 REF.Article

PRUNE BELLY SYNDROME. POSSIBLE GENETIC IMPLICATIONS.GARLINGER P; OTT J.1974; BIRTH DEFECTS ORIGIN ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 8; PP. 173-180; BIBL. 18 REF.Article

THE CEREBROCOSTOMANDIBULAR SYNDROME.LANGER LO JR; HERRMANN J.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 167-170; BIBL. 4 REF.Article

COMPLETE TRISOMY 8 IN A POLYMALFORMED NEWBORNMOERMAN F; FRYNS JP; GODDEERIS P et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 4; PP. 283-285; BIBL. 8 REF.Article

ON THE NATURE OF SYNDROME DELINEATION.COHEN MM JR.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 2; PP. 103-119; ABS. ITAL. FR. ALLEM.; BIBL. 22 REF.Article

THE FAMILIAL OCCURRENCE OF POLAND SYNDROME.SUJANSKY E; RICCARDI VM; MATTHEW AL et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3A; PP. 117-121; BIBL. 14 REF.Article

RADIOLOGICAL CASE OF THE MOUTH.GWINN JL; LEE FA.1976; AMER. J. DIS. CHILD.; U.S.A.; DA. 1976; VOL. 130; NO 10; PP. 1121-1122; BIBL. 5 REF.Article

A NEW FAMILIAL MALFORMATION SYNDROME.AMPOLA MG.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 129-135Article

MEDULLARY SPONGE KIDNEY AND CONGENITAL HEMIHYPERTROPHY: CASE REPORT AND LITERATURE REVIEWHARRIS RE; FUCHS EF; KAEMPF MJ et al.1981; J. UROL.; ISSN 0022-5347; USA; DA. 1981; VOL. 126; NO 5; PP. 676-678; BIBL. 7 REF.Article

A CYTOGENETIC STUDY OF CHILDREN WITH CLINICALLY UNCLASSIFIABLE MULTIPLE CONGENITAL MALFORMATIONS AND MENTAL RETARDATIONNARAHARA K.1981; ACTA MED. OKAYAMA; ISSN 0386-300X; JPN; DA. 1981; VOL. 35; NO 5; PP. 343-355; BIBL. 25 REF.Article

AN AUTOPSY CASE OF D1 (13-15) TRISOMY SYNDROME WITH MULTIPLE CONGENITAL ANOMALIESKIHARA M; KAWAI K; SHIMODA H et al.1979; ACTA PATHOL. JAP.; JPN; DA. 1979; VOL. 29; NO 6; PP. 1013-1022; BIBL. 24 REF.Article

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