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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 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

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

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

TRISOMIE 10 EN MOSAIQUE.VIANELLO MG; GEMME G; BONIOLI E et al.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 2; ABS. ENG/GER; BIBL. 6 REF.Article

FAMILY STUDIES IN CONGENITAL HEART DISEASE. VI. THE ASSOCIATION OF SEVERE OBSTRUCTIVE LEFT LESIONS, VERTEBRAL AND RENAL ANOMALIES: A SECOND FAMILY.KAUFMAN RL; MCALISTER WH; CHEN KUNG HO et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 93-104; BIBL. 15 REF.Article

BETA -HYDROXYISOBUTYRYL COENZYME A DEACYLASE DEFICIENCY: A DEFECT IN VALINE METABOLISM ASSOCIATED WITH PHYSICAL MALFORMATIONSBROWN GK; HUNT SM; SCHOLEM R et al.1982; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1982; VOL. 70; NO 4; PP. 532-538; BIBL. 19 REF.Article

MENTAL RETARDATION AND MULTIPLE CONGENITAL ANOMALIES OF UNKNOWN ETIOLOGY: FREQUENCY OF OCCURRENCE IN SIMILARLY AFFECTED SIBS OF THE PROBANDBARTLEY JA; HALL BD.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 127-137; BIBL. 1 REF.Article

THE CEREBRO-OCULO-FACIO-SKELETAL SYNDROME.SURANA RB; FRAGA JR; SINKFORD SM et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 6; PP. 486-488; BIBL. 4 REF.Article

TRISOMY 22 IN A NEWBORN GIRL WITH MULTIPLE MALFORMATIONSISELIUS L; FAXELIUS G.1978; HEREDITAS; SWE; DA. 1978; VOL. 89; NO 2; PP. 269-271; BIBL. 18 REF.Article

COMPARISON OF EXISTING CLASSIFICATIONS FOR CODING CONGENITAL MALFORMATION AND GENETIC SYNDROMES.LOWRY RB; ROCHELEAU J; KEILLOR L et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3A; PP. 53-59; BIBL. 5 REF.Article

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