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CARACTERISTIQUES DE LA PERSONNALITE DES PARENTS D'ADOLESCENTS ATTEINTS DE SCHIZOPHRENIE JUVENILESHENDEROVA VL.1972; ZH. NEVROPATOL. PSIKHIATR. S. S. KORSAKOVA; S.S.S.R.; DA. 1972; VOL. 72; NO 8; PP. 1195-1203; ABS. ANGL.; BIBL. 42REF.Article

CHORIOIDEREMIE UND FAMILIENBERATUNG = CHOROIDEREMIE ET ENQUETE FAMILIALEKRUEGER KE; MOELLER W; ZERNAHLE K et al.1972; ACTA OPHTHALMOL.; DANEM.; DA. 1972; VOL. 50; NO 6; PP. 782-792; BIBL. 1P.Serial Issue

FAMILIAL EURYBLEPHARONWOLTER JR.1972; J. PEDIATR. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 9; NO 3; PP. 175-176; BIBL. 9REF.Serial Issue

A SURVEY OF MENTALLY DEFECTIVE PARENTS AND THEIR OFFSPRING. = UNE ETUDE DE PARENTS ARRIERES MENTAUX ET DE LEUR DESCENDANCESCALLY BG.1973; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1973; NO 250; PP. 258-262; BIBL. 6REF.; (C.R. IVE CONGR. INT. GENET. HUM.; PARIS; 1971)Conference Paper

FAMILIAL ASSOCIATIONS IN SARCOIDOSIS. A REPORT TO THE RESEARCH COMMITTEE OF THE BRITISH THORACIC AND TUBERCULOSIS ASSOCIATION1973; TUBERCLE; G.B.; DA. 1973; VOL. 54; NO 2; PP. 87-98; ABS. FR. ESP. ALLEM.; BIBL. 2P.1/2Serial Issue

FAMILY WITH PROBABLE ACHONDROGENESIS AND LIPID INCLUSIONS IN FIBROBLASTS = ACHONDROGENESE PROBABLE ET INCLUSIONS LIPIDIQUES DANS LES FIBROBLASTES DANS UNE FAMILLELAXOVA R; OHARA PT; RIDLER MAC et al.1973; ARCH. DIS. CHILDH.; G.B.; DA. 1973; VOL. 48; NO 3; PP. 212-216; BIBL. 7REF.Serial Issue

IGG MONOCLONAL GAMMAPATHY IN THE SISTER OF A PATIENT WITH WALDENSTROEM'S MACROGLOBULINAEMIA = GAMMAPATHIE IGG MONOCLONALE CHEZ LA SOEUR D'UN PATIENT ATTEINT DE MACROGLOBULINEMIE DE WALDENSTROEMFINE JM; LAMBIN P; VALENTIN L et al.1973; BIOMEDICINE; FR.; DA. 1973; VOL. 19; NO 3; PP. 117-121; ABS. FR.; BIBL. 35REF.Serial Issue

3 KINDER MIT CRI-DU-CHAT-SYNDROM = 3 ENFANTS PORTEURS DU SYNDROME DU CRI-DU-CHATPICHLER E; SCHEIBENREITER S.1973; WIEN. MED. WSCHR.; OESTERR.; DA. 1973; VOL. 123; NO 1-2; PP. 19-21; BIBL. 5REF.Serial Issue

A PROPOS D'UN CAS DE MYASTHENIE A DEBUT NEO-NATAL (MYASTHENIE CONGENITALE)CASTANIER L; LELIEVRE GASSIN C.1973; J. MED. STRASBOURG; FR.; DA. 1973; VOL. 4; NO 2; PP. 117-123; ABS. ANGL.; BIBL. 16REF.Serial Issue

FREQUENCE DU PSORIASIS EN FONCTION DE L'AGE1972; VEST. DERMATOL. VENEROL.; S.S.S.R.; DA. 1972; VOL. 46; NO 5; PP. 18-21; ABS. ANGL.; BIBL. 1/2P.Serial Issue

LA NOTION DU HAUT RISQUE DANS LE CANCER DU SEIN DE LA FEMMEGORINS A.1972; C. R. SOC. FR. GYNECOL.; FR.; DA. 1972; VOL. 42; NO 6; PP. 453-464; ABS. ANGL. ESP.; BIBL. 23REF.Article

LE LYMPHOEDEME HEREDITAIRE DE MILROY-MEIGE-NONNE. (A PROPOS D'UNE OBSERVATION FAMILIALE)RUSSEIL JC.1972; LYON; ASSOC. CORP. ETUD. MED.; DA. 1972; PP. 1-42; BIBL. 7P.; (THESE DOCT. MED.; UNIV. CLAUDE BERNARD-LYON)Thesis

MESURES D'AGGLUTINATION QUANTITATIVE DES PHENOTYPESB FAIBLESLOPEZ M; LE MEUD J; GERBAL A et al.sdNOW. REV. FR. HEMATOL.; FR.; DA. 197; VOL. 13; NO 1; PP. 107-118; ABS. ANGL.; BIBL. 12REF.Serial Issue

FANCONI'S ANAEMIABEARD MEJ; YOUNG DE; BATEMAN CJT et al.1973; QUART. J. MED.; G.B.; DA. 1973; VOL. 42; NO 166; PP. 403-422; BIBL. 1P.Serial Issue

HAEMOGLOBIN H DISEASE IN A TURKISH FAMILY = HEMOGLOBINOSE H DANS UNE FAMILLE TURQUEOZSOYLU S; ISIK K.1973; SCAND. J. HAEMATOL.; DENM.; DA. 1973; VOL. 10; NO 1; PP. 54-58; BIBL. 1P.Serial Issue

HEREDOBIOLOGICAL PROBLEMS RELATED WITH THYROID AUTOIMMUNITY = ASPECTS BIOLOGIQUES HEREDITAIRES DE L'AUTO-IMMUNITE THYROIDIENNESIMIONESCU L; SAHLEANU V.1973; REV. ROUMAINE ENDOCRINOL.; ROUMAN.; DA. 1973; VOL. 10; NO 2; PP. 121-131Article

POLYMORPHISM OF HUMAN C-BAND HETEROCHROMATIN. I. FREQUENCY OF VARIANTS = POLYMORPHISME DE L'HETEROCHROMATINE DES BANDES C HUMAINES. I. FREQUENCE DES VARIANTESCRAIG HOLMES AP; MOORE FB; SHAW MW et al.1973; AMER. J. HUM. GENET.; U.S.A.; DA. 1973; VOL. 25; NO 2; PP. 181-192; BIBL. 17REF.Serial Issue

VALUE OF TWIN STUDIES IN DERMATOLOGICAL GENETICS = VALEUR DE L'ETUDE DES JUMEAUX EN DERMATOLOGIE GENETIQUECAVALIERI R.1973; INTERNATION. J. DERMATOL.; U.S.A.; DA. 1973; VOL. 12; NO 1; PP. 29-34; BIBL. 7REF.Serial Issue

SCLEROSE EN PLAQUES ET FAMILLEBOUCHE B; BELANGER C; SAINT HILAIRE JM et al.1972; LYON MEDITERR. MED.; FR.; DA. 1972; VOL. 8; NO 23; PP. 2209-2224 (9 P.); BIBL. 34 REF.Serial Issue

ABERRATIONS CHROMOSOMIQUES CHEZ LES PARENTS DANS DES CAS D'AVORTEMENTS SPONTANES REPETESKULAZHENKO VP; LAZYUK GI; LEVCHENKO NN et al.1972; GENETIKA; S.S.S.R.; DA. 1972; VOL. 8; NO 7; PP. 154-164; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

ABSENCE DE DIABETE CHEZ LE JUMEAU UNIVETELLIN D'UN DIABETIQUE1973; REV. FR. ENDOCRINOL. CLIN.; FR.; DA. 1973; VOL. 14; NO 1; PP. 61-64; ABS. ANGL.; BIBL. 7REF.Serial Issue

UN CAS DE SYNDROME DU CRI DU CHAT AVEC CARYOTYPE INHABITUEL CHEZ LE PEREBOGOMAZOV EA; AVER'YANOV YU N; ZOTOV VV et al.1973; GENETIKA; S.S.S.R.; DA. 1973; VOL. 9; NO 1; PP. 174-176; H.T. 2; ABS. ANGL.; BIBL. 4REF.Serial Issue

STUDIES ON RELATIVES OF PATIENTS WITH GLAUCOMA SIMPLEX AND PATIENTS WITH PSEUDO EXFOLIATION OF THE LENS CAPSULE = ETUDES DES PARENTS DE SUJETS PRESENTANT UN GLAUCOME SIMPLE ET DE SUJETS PRESENTANT UNE PSEUDO EXFOLIATION DE LA CAPSULE CRISTALLINIENNE1972; ACTA OPHTALMOL.; DANEM.; DA. 1972; VOL. 50; NO 2; PP. 255-261; BIBL. 14 REF.Serial Issue

Y FAMILY STUDY. HERITABLE VARIATION IN THE LENGTH OF THE HUMAN Y CHROMOSOME = ETUDE FAMILIALE SUR L'Y. VARIATION HEREDITAIRE DE LA LONGUEUR DU CHROMOSOME Y HUMAINMCHENZIE WH; HOSTETTER TL; LUBS HA et al.1972; AMER. J. HUM. GENET.; U.S.A.; DA. 1972; VOL. 24; NO 6, PART1; PP. 686-693; BIBL. 1P.Serial Issue

FREQUENCE DU SYNDROME DOWN DANS UNE FAMILLEDOBRZANSKA A; KOSTRZEWSKI J.1971; ANN. UNIV. MARIAECURIE-SKLODOWSKA, D; POLOGNE; DA. 1971; VOL. 26; PP. 137-144; H.T. 5; ABS. RUSSE ANGL.; BIBL. 23REF.Serial Issue

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