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Syndrome oro-facio-digital type I de Papillon-Léage et Psaume: à propos d'un cas = Orodigito facial type I. Papillon-Leage and Psaume syndrome: one caseGALABERT, J; BOURDONCLE, A.Actualités odonto-stomatologiques. 1984, Vol 38, Num 148, pp 745-755, issn 0001-7817Article

Diagnostic cosmétique et fonctionnel dans les dysmorphoses faciales verticales = Aesthetic and functional diagnosis of facial deformityACHARD, R; GUILLAUBEY, M.Lyon méditerranée médical. 1985, Vol 21, Num 8, pp 9815-9820, issn 0399-032X, 4 p.Article

MATERNAL EFFECTS IN HUMAN CLEFT LIP AND PALATE.BINGLE GJ; NISWANDER JD.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 29; NO 6; PP. 605-609; BIBL. 23 REF.Article

DOMINANT INHERITANCE OF FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROMELAMPERT RP.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 4; PP. 255-258; BIBL. 6 REF.Article

BRIEF CLINICAL REPORT: FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROMEHURST D; JOHNSON DF.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 3; PP. 255-258; BIBL. 12 REF.Article

THE GENETIC ASPECTS OF FACIAL ABNORMALITIES.GORLIN RJ; BOGGS WS.1977; ADV. HUM. GENET.; U.S.A.; DA. 1977; VOL. 8; PP. 235-246; BIBL. 8 P.Article

Nanisme avec vertèbres hautes et étroites: deux nouvelles observations = Dwarfism with high narrow vertebrae. Two new casesROCHICCIOLI, P; MALPUECH, G.Annales de pédiatrie (Paris). 1983, Vol 30, Num 9, pp 709-712, issn 0066-2097Article

Measuring Attentional Bias to Peripheral Facial DeformitiesISHII, Lisa; CAREY, John; BYRNE, Patrick et al.The Laryngoscope. 2009, Vol 119, Num 3, pp 459-465, issn 0023-852X, 7 p.Article

INDICATION DU SIEGE DES OSTEOTOMIES MANDIBULAIRES DANS LES CORRECTIONS DES DYSMORPHOSESVESSE M; BENOIST M; COURTOIS B et al.1983; REVUE DE STOMATOLOGIE ET DE CHIRURGIE MAXILLO-FACIALE; ISSN 0035-1768; FRA; DA. 1983; VOL. 84; NO 2; PP. 67-72; ABS. ENG; BIBL. 27 REF.Article

THE PUPPET-LIKE SYNDROME OF ANGELMANDOOLEY JM; BERG JM; PAKULA Z et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 7; PP. 621-624; BIBL. 12 REF.Article

ABNORMAL SKIN FIBROBLAST CYTOGENETICS IN FOUR DYSMORPHIC PATIENTS WITH NORMAL LYMPHOCYTE CHROMOSOMESFAGON RA; HALL JG; DAVENPORT SLH et al.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 1; PP. 54-61; BIBL. 33 REF.Article

POTTER-SYNDROM. = SYNDROME DE POTTERSTECHELE U; STRAUB E.1978; KLIN. PAEDIATR.; DTSCH.; DA. 1978; VOL. 190; NO 2; PP. 139-146; ABS. ANGL.; BIBL. 26 REF.Article

GIGANTISME CEREBRAL: DEUX CAS FAMILIAUX.KRAUEL X; BERGER R; AMIEL TISON C et al.1977; J. GENET. HUM.; SUISSE; DA. 1977; VOL. 25; NO 3; PP. 205-214; ABS. ANGL. ALLEM.; BIBL. 1 P. 1/2Article

RING CHROMOSOME 15 IN CHILD WITH A MINOR DYSMORPHISM OF PHENOTYPE.RUMENIE L; JOKSIMOVIC I; ANAF M et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 187-188; BIBL. 5 REF.Article

THE LONG FACE SYNDROME: VERTICAL MAXILLARY EXCESS.SCHENDEL SA; EISENFELD J; BELL WH et al.1976; AMER. J. ORTHODONT.; U.S.A.; DA. 1976; VOL. 70; NO 4; PP. 398-408; BIBL. 26 REF.Article

THE WEAVER SYNDROME: A RARE TYPE OF PRIMORDIAL OVERGROWTHMASEWSKI F; RANKE M; KEMPERDICK H et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 137; NO 3; PP. 277-282; BIBL. 7 REF.Article

THE BOERJESON-FORSSMAN-LEHMANN SYNDROME: A NEW CASEVEALL RM; BRETT EM; RIVINUS TM et al.1979; J. MENTAL DEFIC. RES.; GBR; DA. 1979; VOL. 23; NO 4; PP. 231-242; BIBL. 23 REF.Article

SYNDROME DE POTTER ET CARYOTYPE 46,XX CHEZ UN NOUVEAU-NE DE PHENOTYPE MASCULINFAUGERAS C; JOLY JB; LALEU J et al.1979; REV. MED. LIMOGES; FRA; DA. 1979; VOL. 10; NO 1; PP. 55-58; BIBL. 17 REF.Article

SINDROME DI FREEMAN-SHELDON CON RITARDO MENTALE = SYNDROME DE FREEMAN-SHELDON AVEC RETARD MENTALSILENGO MC; DAVI GF; BIANCO R et al.1982; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1982; VOL. 34; NO 6; PP. 277-280; ABS. ENG; BIBL. 18 REF.Article

VARIABILITA CLINICA DELLA SINDROME DI POTTER: PRESENTAZIONE DI DUE CASI = VARIABILITE CLINIQUE DU SYNDROME DE POTTER: PRESENTATION DE 2 CASTORRICELLI M; DELUCA L; PANSINI L et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 16; PP. 1001-1006; ABS. ENG; BIBL. 19 REF.Article

FACIAL DEFORMITY: A PREVENTABLE DISEASERUBIN RM.1979; ANGLE ORTHODONTIST; USA; DA. 1979; VOL. 49; NO 2; PP. 98-103; BIBL. 23 REF.Article

CONJONCTION CHIRURGICO ORTHOPEDIQUE DANS LE TRAITEMENT DES DYSMORPHIES VERTICALES GRAVES DE L'ADULTEMICHELET FX; GIRONET J; BAUME L et al.1979; REV. ODONTO-STOMATOL. MIDI FR.; FRA; DA. 1979; VOL. 37; NO 3; PP. 187; ABS. ENGArticle

ZEREBRALER GIGANTISMUS (SOTOS-SYNDROM). = LE GIGANTISME CEREBRAL (SYNDROME DE SOTOS)LACHMANN D; FRISH H; POLZ E et al.1977; PAEDIATR. U. PAEDOL.; OESTERR.; DA. 1977; VOL. 12; NO 4; PP. 404-409; ABS. ANGL.; BIBL. 12 REF.Article

HISTORICAL BACKGROUND AND EVIDENCE FOR DOMINANT INHERITANCE OF THE KLEIN-WAARDENBURG SYNDROME (TYPE III)KLEIN D.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 231-239; BIBL. 2 P.Article

LA SINDROME DI POTTER: PRESENTAZIONE DI UN CASO CON ALCUNE PARTICOLARITA ED ESAME DELLA LETTERATURA PIU RECENTE = LE SYNDROME DE POTTER. PRESENTATION D'UN CAS AVEC QUELQUES PARTICULARITES ET REVUE DE LA LITTERATURE RECENTESCALERCIO A; GIUSTIZIERI A; CECCARELLI G et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 13; ENG.; PP. 837-844; BIBL. 25 REF.Article

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