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Results 1 to 25 of 2059

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HEREDITARY CHILDHOOD HEARING LOSS AND INTEGUMENTARY SYSTEM DISEASE = SURDITE HEREDITAIRE DE L'ENFANT ET MALADIE DU SYSTEME TEGUMENTAIREKONIGSMARK BW.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 80; NO 6; PP. 909-919; BIBL. 1P.Serial Issue

A CARDIO-FACIAL-SKELETAL SYNDROME = SYNDROME CARDIO-FACIO-SQUELETTIQUE1972; AMER. J. ROENTGENOL. RADIUM THERAPY NUCL. MED.; U.S.A.; DA. 1972; VOL. 116; NO 3; PP. 634-639; BIBL. 18REF.Serial Issue

COEUR ET SURDITES GENETIQUESPERNOT C; HENRY M; DEBRUILLE C et al.1973; MED. INFANT.; FR.; DA. 1973; VOL. 80; NO 1; PP. 115-133; BIBL. 2P.1/2Serial Issue

SINDROME DE RUBINSTEIN-TAYBI. (ESTUDIO SOBRE OCHO CASOS) = SYNDROME DE RUBINSTEIN-TAYBI. (ETUDE SUR 8 CAS)DEL CASTILLO F; LOPEZ MARTIN V; RODRIGUEZ COSTA T et al.1972; ARCH. NEUROBIOL.; ESP.; DA. 1972; VOL. 35; NO 5; PP. 425-452; ABS. FR. ANGL. ALLEM.; BIBL. 1 P. 1/2Serial Issue

OCULAR MANIFESTATIONS OF THE MECKEL SYNDROMEMACRAE DW; HOWARD RO; ALBERT DM et al.1972; ARCH. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 88; NO 1; PP. 106-113; BIBL. 13REF.Serial Issue

HYPOPLASIE DER RECHTEN LUNGE MIT CYSTISCHEN BRONCHIEKTASIEN UND DEXTROVERSIO CORDIS (ZUR DIFFERENTIALDIAGNOSE DES KARTAGENER-SYNDROMS) = HYPOPLASIE DU POUMON DROIT AVEC BRONCHECTASIES KYSTIQUES ET DEXTROCARDIE (DIAGNOSTIC DIFFERENTIEL DU SYNDROME DE KARTAGENER)KARTAGENER M; SPOENDLIN H.1972; PNEUMOLOGIE; DTSCH.; DA. 1972; VOL. 148; NO 1; PP. 1-6; ABS. ANGL.; BIBL. 2 REF.Serial Issue

MARFAN'S SYNDROME AND MENTAL SUBNORMALITYELSARRAG ME; QUINN M.1972; BRIT. J. MENTAL SUBNORM.; G.B.; DA. 1972; VOL. 18; NO 1; PP. 46-47; BIBL. 4REF.Serial Issue

ANOMALIES CONGENITALES SOMATIQUES DANS UN SYNDROME DE DYSGENESIE GONADIQUEGALAZKA A; GLEBOWSKA H; ORLESKA I et al.1972; WIADOM. LEK.; POLSKA; DA. 1972; VOL. 25; NO 20; PP. 1827-1831; ABS. RUSSE ANGL.; BIBL. 13REF.Serial Issue

LA CONSULENZA EUGENICA DOPO LA NASCITA DI UN NEONATO CON MALFORMAZIONI CONGENITE = LA CONSULTATION EUGENIQUE APRES LA NAISSANCE D'UN NOUVEAU-NE AYANT DES MALFORMATIONS CONGENITALESBEOLCHINI PE.1972; MINERVA MED.; ITAL.; DA. 1972; VOL. 63; NO 85; PP. 4660-4664; BIBL. 19 REF.Serial Issue

SINDROME DE CORNELIA DE LANGE = SYNDROME DE CORNELIA DE LANGEWERNECK LC; MARCALLO FA.1972; ARQ. NEURO-PSIQUIATR.; BRAS.; DA. 1972; VOL. 30; NO 4; PP. 353-357; ABS. ANGL.; BIBL. 14REF.Serial Issue

LE GENETICIEN ET LES MALFORMATIONSDESSEMOND M.1976; REV. PRATICIEN; FR.; DA. 1976; VOL. 26; NO 7; PP. 491-503 (9P.); ABS. ANGL.Article

BLOOM'S SYNDROME = SYNDROME DE BLOOMBLOOM D; GERMAN J.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 16; NO 4; PP. 361Serial Issue

HEMIHYPERTROPHIE CONGENITALE ASSOCIEE A UNE ANOMALIE DES ARCS AORTIQUES ET A DIVERSES MALFORMATIONS SQUELETTIQUES, CUTANEES, OCULAIRESHENRY M; LOUIS JP; HOEFFEL JC et al.1972; ANN. MED. NANCY; FR.; DA. 1972; VOL. 9; PP. 1111-1120 (8P.); BIBL. 26 REF.Serial Issue

MALFORMAZIONI E DISMORFIE EXTRACARDIACHE ASSOCIATE A CARDIOPATIA CONGENITA. CONSIDERAZIONI SU DI UN CASO E DISCUSSIONE SUI RAPPORTI TRA SINDROME DI NOONAN E STATI PARATURNERIANI = MALFORMATIONS ET DYSMORPHIE EXTRACARDIAQUES ASSOCIEES A UNE CARDIOPATHIE CONGENITALE. NOTES SUR UN CAS ET DISCUSSION DES RAPPORTS ENTRE SYNDROME DE NOONAN ET ETATS TURNEROIDESPILOTTI G; CASTELLI G; RICCI C et al.1972; MINERVA PEDIATR.; ITAL.; DA. 1972; VOL. 24; NO 41; PP. 2059-2071; ABS. ANGL.; BIBL. 2P.Serial Issue

THE AARSKOG SYNDROMEFURUKAWA CT; HALL BD; SMITH DW et al.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 81; NO 6; PP. 1117-1122; BIBL. 15 REF.Serial Issue

COEUR ET MALADIES GENETIQUES HEREDITAIRESEMERIT I.1973; VIE MED.; FR.; DA. 1973; VOL. 54; NO 1; PP. 21-32 (8 P.); ABS. ANGL.; BIBL. 16 REF.Serial Issue

CHROMOSOMAL ANOMALY ASSOCIATED WITH CORNELIA DE LANGE'S SYNDROME = UNE ANOMALIE CHROMOSOMIQUE ASSOCIEE AU SYNDROME DE CORNELIA DE LANGESZEMERE G; GODO B; OSVATH P et al.1972; ACTA PAEDIATR. ACAD. SCI. HUNGAR.; HONGR.; DA. 1972; VOL. 13; NO 1; PP. 51-55; ABS. RUSSE; BIBL. 13 REF.Serial Issue

ARACHNODACTYLY (MARFAN'S SYNDROME) WITH XYY KARYOTYPE = ARACHNODACTYLIE (SYNDROME DE MARFAN) AVEC CARYOTYPE XYYDIGNAN PSJ; KREINES K; SOUKUP S et al.1972; AMER. J. DIS. CHILD.; U.S.A.; DA. 1972; VOL. 124; NO 2; PP. 266-270; BIBL. 37REF.Serial Issue

PRUNE BELLY SYNDROME = LE SYNDROME D'ABSENCE CONGENITALE DE MUSCULATURE ABDOMINALEHARLEY LM; YOUCHEN; RATTNER WH et al.1972; J. UROL.; U.S.A.; DA. 1972; VOL. 108; NO 1; PP. 174-176; BIBL. 16REF.Serial Issue

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

HYPERTELORISME ET MALFORMATIONS ASSOCIEESFERRIER PE; FREUND MM.1974; REV. OTO-NEURO-OPHTALMOL.; FR.; DA. 1974; VOL. 46; NO 5; PP. 457-459; BIBL. 7REF.; (XXXIIIE. REUN. ANNU. GROUPE ONO NEUROCHIR. SUISSE ROMANDE; GENEVE; 1973)Conference Paper

CARDIOMYOPATHY IN NOONAN'S SYNDROME. REPORT OF 3 CASES = CARDIOMYOPATHIE DANS LE SYNDROME DE NOONAN. PRESENTATION DE 3 CASPHORNPHUTKUL C; ROSENTHAL A; NADAS AS et al.1973; BRIT. HEART J.; G.B.; DA. 1973; VOL. 35; NO 1; PP. 99-102; BIBL. 10REF.Serial Issue

GENETIC DISORDERS ASSOCIATED WITH MENTAL RETARDATION. CLINICAL ASPECTS = MALADIES GENETIQUES ASSOCIEES A UNE ARRIERATION MENTALE. ASPECTS CLINIQUESSCOTT CI JR; THOMAS GH.1973; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1973; VOL. 20; NO 1; PP. 121-140; BIBL. 4P.1/2Serial Issue

DYSGENETISCHE NEBENBEFUNDE BEI DEN ZEPHALAZELEN = LES ASSOCIATIONS DYSGENETIQUES DANS LES CEPHALOCELESIIZUKA J.1973; Z. KINDERCHIR. GRENZGEB.; DTSCH.; DA. 1973; VOL. 12; NO 1; PP. 16-27; ABS. ANGL. FR. ESP.; BIBL. 1 P. 1/2Serial Issue

ANOMALIES URINAIRES ET AGENESIE DES MUCLES DE LA PAROI ABDOMINALE. PRUNE-BELLY SYNDROMEMARC J; COMTE B; DILHUYDY JM et al.1973; J. RADIOL. ELECTRO. MED. NUCL.; FR.; DA. 1973; VOL. 54; NO 5; PP. 379-382; ABS. ANGL.; BIBL. 9REF.Serial Issue

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