Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("FACIAL DEFORMITY")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 612

  • Page / 25
Export

Selection :

  • and

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

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

THE NOONAN SYNDROMESANCHEZ CASCOS A.1983; EUROPEAN HEART JOURNAL; ISSN 0195-668X; GBR; DA. 1983; VOL. 4; NO 4; PP. 223-229; BIBL. 22 REF.Article

PARTIAL 11Q TRISOMY SYNDROMEPIHKO H; THERMAN E; UCHIDA IA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 129-134; BIBL. 33 REF.Article

PARTIAL 8P-SYNDROMEPATIL SR; HANSON JW.1980; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1980; VOL. 28; NO 4; PP. 123-129; ABS. FRE; BIBL. 12 REF.Article

THE WEAVER-SMITH SYNDROMEGEMME G; BONIOLI E; RUFFA G et al.1980; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1980; VOL. 97; NO 6; PP. 962-964; BIBL. 6 REF.Article

L'INTUBATION TRACHEALE CHEZ LES ENFANTS ATTEINTS DE DYSMORPHIES CRANIO-FACIALES CONGENITALES: DETECTION PRE-OPERATOIRE DES DIFFICULTESDELEGUE L; ROSENBERG S; GHNASSIA MD et al.1980; ANESTH. ANAL. REANIM.; FRA; DA. 1980; VOL. 37; NO 3-4; PP. 133-138; ABS. ENG; BIBL. 3 REF.Article

MALADIE DE DEJERINE-SOTTAS CHEZ L'ENFANT: A PARTIR D'UNE OBSERVATION PARTICULIERE DE NEUROPATHIE HYPERTROPHIQUE AVEC DYSMORPHIE FACIALELANFANT GOUTAZ MARIE PIERRE.1980; ; FRA; DA. 1980; 71; 108-XXI P.: ILL.; 30 CM; BIBL. 146 REF.; TH.: MED./PARIS 7/1980Thesis

A TERMINAL LONG ARM DELETION OF CHROMOSOME 16 IN A DYSMORPHIC INFANT: 46, XY, DEL (16) (Q22)TAYSI K; FISHMAN M; SEKHON GS et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 343-347; BIBL. 4 REF.Article

ANNEAU DU CHROMOSOME 4. II. SANS DYSMORPHIE FACIALE.CHAVIN COLIN F; TURLEAU C; LIMAL JM et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 105-109; ABS. ANGL.; BIBL. 12 REF.Article

THE W SYNDROME. STUDIES OF MALFORMATION SYNDROMES OF MAN. XXVIII.PALLISTER PD; HERRMANN J; SPRANGER JW et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 7; PP. 51-60; BIBL. 3 REF.Article

  • Page / 25