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Results 1 to 25 of 5649

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MELORHEOSTOSEALLAIN O; FAURE C.1980; FEUILL. PRAT.; FRA; DA. 1980; VOL. 4; NO 11; PP. 405-406; BIBL. 4 REF.Article

L'OSTEOPOECILIE. A PARTIR D'UN CAS. PARTICULARITES ET PROBLEMES ACTUELSPEYTAVY MONIQUE.1979; ; FRA; BORDEAUX: ED. BERGERET; DA. 1979; 124; 74 P.: ILL; BIBL. 98 REF.; TH.: MED./BORDEAUX 2/1979Thesis

ATELOSTEOGENESISMAROTEAUX P; SPANGER J; STANESCU V et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 1; PP. 15-25; BIBL. 9 REF.Article

METACHONDROMATOSISBEALS RK.1982; CLIN. ORTHOP. RELAT. RES.; ISSN 0009-921X; USA; DA. 1982; NO 169; PP. 167-170; BIBL. 9 REF.Article

THERAPEUTIC PROBLEMS IN FAMILIAL POLY-EPIPHYSEAL DYSCHONDROPLASIACIGALA F; SERVODIO IAMMARRONE C.1982; ITAL. J. ORTHOP. TRAUMATOL.; ISSN 506575; ITA; DA. 1982; VOL. 8; NO 2; PP. 153-158; BIBL. 14 REF.Article

ROENTGEN ROUNDS. LIILING D; GILULA LA.1981; ORTHOP. REV.; ISSN 0094-6591; USA; DA. 1981; VOL. 10; NO 2; PP. 125-128; BIBL. 6 REF.Article

OSTEOGENESE IMPARFAITE TARDIVERICHARD M; COURPRON P.1980; LYON MED.; ISSN 0024-7790; FRA; DA. 1980; VOL. 244; NO 13; PP. 35-41; ABS. ENG; BIBL. 46 REF.Article

DIE DYSCHONDROSTEOSE LERI-WEILL = LA DYSCHONDROSTEOSE DE LERI-WEILLKOCH HL.1983; ROEFOE. FORTSCHRITTE AUF DEM GEBIETE DER ROENTGENSTRAHLEN UND DER NUKLEARMEDIZIN; ISSN 0340-1618; DEU; DA. 1983; VOL. 138; NO 5; PP. 603-606; BIBL. 15 REF.Article

THE CAMPOMELIC SYNDROME: REVIEW, REPORT OF 17 CASES, AND FOLLOW-UP ON THE CURRENTLY 17-YEAR-OLD BOY FIRST REPORTED BY MAROTEAUX ET AL. IN 1971HOUSTON CS; OPITZ JM; SPRANGER JW et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 3-28; BIBL. 4 P.Article

LA MALADIE CONGENITALE DES EPIPHYSES PONCTUEES. DIFFICULTES DIAGNOSTIQUES, INCERTITUDES NOSOLOGIQUES: A PROPOS DE 5 OBSERVATIONS CLINIQUESTROUILLARD PERROT MICHEL.1980; ; FRA; DA. 1980; 65 P.; 30 CM; BIBL. 37 REF.; TH.: MED./PARIS 6/1980/122Thesis

LA MALADIE DES EPIPHYSES PONCTUEES (A PROPOS DE 6 OBSERVATIONS)FALL M; NIANG I; KUAKUVI N et al.1979; DAKAR MED.; SEN; DA. 1979; VOL. 24; NO 4; PP. 377-384; ABS. ENG; BIBL. 19 REF.Article

LA SINDROME DI LARSEN: DESCRIZIONE DI UN CASO ION ECCEZIONALE DISMATURITA SCHELETRICA = LE SYNDROME DE LARSEN: DESCRIPTION D'UN CAS AVEC DYSMATURITE SQUELETTIQUE EXCEPTIONNELLECOLOMBO ML; TOSI MT; MAGNETTI L et al.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 24; PP. 1765-1774; ABS. ENG; BIBL. 17 REF.Article

CONTRIBUTION A L'ETUDE DU NANISME THANATOPHORE (A PROPOS DE 5 OBSERVATIONS)GENARD PIQUET GAUTHIER MARIE CHRISTINE.1979; ; FRA; DA. 1979; 123; 113 P.-22 PL.: ILL.; 30 CM; BIBL. 81 REF.; TH.: MED./LYON 1/1979Thesis

L'OSTEOGENESE IMPARFAITE TARDIVE. CONNAISSANCES ACTUELLES (1967-1978)RICHARD MERMET MARYSE.1979; ; FRA; DA. 1979; 140; 201 P.: ILL.; 30 CM; BIBL. 34 P.; TH.: MED./LYON 1/1979Thesis

OSTEOGENESIS IMPERFECTA CONGENITA; HISTOIRE DE DEUX CASTITUS H.1979; MED. AFR. NOIRE; ISSN 0465-4668; SEN; DA. 1979; NO SPEC.; PP. 425-428; BIBL. 7 REF.Conference Paper

ABNORMAL ALPHA 2-CHAIN IN TYPE I COLLAGEN FROM A PATIENT WITH A FORM OF OSTEOGENESIS IMPERFECTABYERS PH; SHAPIRO JR; ROWE DW et al.1983; JOURNAL OF CLINICAL INVESTIGATION; ISSN 0021-9738; USA; DA. 1983; VOL. 71; NO 3; PP. 689-697; BIBL. 43 REF.Article

EDITORIAL COMMENT: GENETIC HETEROGENEITY OF SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA.SPRANGER JW; MAROTEAUX P.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 241-242; BIBL. 4 REF.Article

ROENTGEN ROUNDSMCDONALD JE; MURPHY WA; GILULA LA et al.1980; ORTHOP. REV.; ISSN 0094-6591; USA; DA. 1980; VOL. 9; NO 8; PP. 79-82; BIBL. 12 REF.Article

A POSSIBLY NEW FORM OF FAMILIAL BONE DYSPLASIA RESEMBLING DYSCHONDROSTEOSISFASANELLI S; IANNACCONE G; BELLUSSI A et al.1983; PEDIATRIC RADIOLOGY; ISSN 0301-0449; DEU; DA. 1983; VOL. 13; NO 1; PP. 25-31; BIBL. 14 REF.Article

CHONDRODYSTROPHIC MYOTONIA (SCHWARTZ-JAMPEL SYNDROME): REPORT OF A NEW CASE AND FOLLOW-UP OF PATIENTS INITIALLY REPORTED IN 1969EDWARDS WC; ROOT AW.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 1; PP. 51-56; BIBL. 13 REF.Article

NORMAL LIPID COMPOSITION OF FIBROBLASTS FROM A CASE OF TYPE II ACHONDROGENESISLE LOUS M; HORS CAYLA MC; HENDRICKX GFM et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 2; PP. 159-160; BIBL. 12 REF.Article

A PROPOS D'UN CAS D'ACHONDROGENESESROUJI TONY.1979; ; FRA; DA. 1979; 5; 83-X P.-7 PL.; 30 CM; BIBL. 97 REF.; TH.: MED./NANCY 1/1979Thesis

A CASE OF NEW CHONDRODYSTROPHYKOIDE T; KATAYAMA H; SUMI Y et al.1983; PEDIATRIC RADIOLOGY; ISSN 0301-0449; DEU; DA. 1983; VOL. 13; NO 2; PP. 102-105; BIBL. 4 REF.Article

PATHOLOGICAL ANATOMY OF THE HANDS IN APERT'S SYNDROMEGREEN SM.1982; JOURNAL OF HAND SURGERY; ISSN 0363-5023; USA; DA. 1982; VOL. 7; NO 5; PP. 450-453; BIBL. 2 REF.Article

SPONDYLOHUMEROFEMORAL HYPOPLASIA (GIANT CELL CHONDRODYSPLASIA): A NEONATALLY LETHAL SHORT-LIMB SKELETAL DYSPLASIASILLENCE DO; LACHMANN RS; JENKINS T et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 1; PP. 7-14; BIBL. 8 REF.Article

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