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Results 1 to 25 of 53

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DISPROPORTIONATE MICROMELIA (DMM): AN INCOMPLETE DOMINANT MOUSE DWARFISM WITH ABNORMAL CARTILAGE MATRIXBROWN KS; CRANLEY RE; GREENE R et al.1981; J. EMBRYOL. EXP. MORPHOL.; ISSN 0022-0752; GBR; DA. 1981; VOL. 62; PP. 165-182; BIBL. 2 P.Article

Acromicric dysplasiaMAROTEAUX, P; STANESCU, R; STANESCU, V et al.American journal of medical genetics. 1986, Vol 24, Num 3, pp 447-459, issn 0148-7299Article

Craniomicromelic Syndrome: First Report in a MaleGAMBHIR, Prakash S; GAMBHIR, Sunita.American journal of medical genetics. Part A. 2011, Vol 155, Num 3, pp 586-588, issn 1552-4825, 3 p.Article

DAS GOTTREN-SYNDROM UNTER ZAHNAERZTLICHER SICHT: EIN FALLBERICHT = LE SYNDROME DE GOTTRON DU POINT DE VUE DU STOMATOLOGISTE: UNE OBSERVATIONGUNTHER HM; SITZMANN F.1978; DTSCH. ZAHNAERZTL. Z.; DEU; DA. 1978; VOL. 33; NO 12; PP. 873-875; ABS. ENG; BIBL. 11 REF.Article

MICROMELIA, POLYSYNDACTYLY, MULTIPLE MALFORMATIONS, AND FRAGILE BONES IN A STILLBORN CHILDCARPENTER BF; HUNTER AGW.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 311Article

Limb deformity induced in chick embryo by hydroxyureaIWAMA, M; SAKAMOTO, Y; HONDA, A et al.Journal of pharmacobio-dynamics. 1983, Vol 6, Num 11, pp 836-843, issn 0386-846XArticle

OpsismodysplasiaLEWIS, Leslie Edward S; RAMESH BHAT, Y; NAIK, Prashant et al.Indian journal of pediatrics. 2010, Vol 77, Num 5, pp 567-568, issn 0019-5456, 2 p.Article

AUTOSOMAL RECESSIVE MICROCEPHALY AND MICROMELIA IN CREE INDIANSIVES EJ; HOUSTON CS.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 3; PP. 351-360; BIBL. 9 REF.Article

HETEROGENEITY OF NONLETHAL SEVERE SHORT-LIMBED DWARFISM.ROMEO G; ZONANA J; RIMOIN DL et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 6; PP. 918-923; BIBL. 17 REF.Article

GREBE CHONDRODYSPLASIA AND SIMILAR FORMS OF SEVERE SHORT-LIMBED DWARFISM.ROMEO G; ZONANA J; LACHMAN RS et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 109-115; BIBL. 10 REF.Article

HETEROGENEITY IN THE CAMPOMELIC SYNDROMES.ABOL KHAJAVI; LACHMAN R; RIMOIN D et al.1976; RADIOLOGY; U.S.A.; DA. 1976; VOL. 120; NO 3; PP. 641-647; BIBL. 25 REF.Article

L'HYPERTRICHOSE DU SYNDROME MALFORMATIF DE CORNELIA DE LANGE.VISSIAN L; ROVINSKI J.1978; ANN. DERMATOL. VENEREOL.; FR.; DA. 1978; VOL. 105; NO 4; PP. 427-430; ABS. ANGL.; BIBL. 9 REF.Article

ASSOCIAZIONE DI SINDROME DI CORNELIA DE LANGE, MORBO DI PERTHES E ALTERAZIONI SCHELETRICHE MULTIPLE: DA ROSOLIA CONGENITA. = ASSOCIATION DE SYNDROME DE CORNELIA DE LANGE, MALADIE DE PERTHES ET ALTERATIONS SQUELETTIQUES MULTIPLES: PAR RUBEOLE CONGENITALE.GIULO GIORDANO G; CAPECE G; COCCO U et al.1978; PEDIATRIA; ITA; DA. 1978; VOL. 86; NO 3; PP. 375-387; ABS. FRE/ENG/GER/SPA; BIBL. 1 P.Article

SYNDROME OF FAMILIAL DWARFISM AND HIGH PLASMA IMMUNOREACTIVE GROWTH HORMONE (IR-HGH)-LARON TYPE DWARFISM.LARON Z.1977; PAEDIATRICIAN; SWITZ.; DA. 1977; VOL. 6; NO 2; PP. 106-117; BIBL. 2 P. 1/2Article

Pulmonary hypoplasia associated with reduced thoracic space in mice with disproportionate micromelia (DMM)FOSTER, M. J; CALDWELL, A. P; STAHELLI, J et al.The Anatomical record. 1994, Vol 238, Num 4, pp 454-462, issn 0003-276XArticle

Hand and foot length in Prader-Willi syndromeHUDGINS, L; CASSIDY, S. B.American journal of medical genetics. 1991, Vol 41, Num 1, pp 5-9, issn 0148-7299Article

CORNELIA DE LANGE SYNDROME: OCCURRENCE IN TWINSWATSON A.1979; AUSTRALAS. J. DERMATOL.; AUS; DA. 1979; VOL. 20; NO 1; PP. 7-9; BIBL. 7 REF.Article

SPURS OF THE MANDIBLE AND SUPRACONDYLAR PROCESS OF THE HUMERUS IN CORNELIA DE LANGE SYNDROME.CURTIS JA; O'HARA AE; CARPENTER GC et al.1977; AMER. J. ROENTGENOL.; U.S.A.; DA. 1977; VOL. 129; NO 1; PP. 156-158; BIBL. 13 REF.Article

UN CASO DI MALFORMAZIONI MULTIPLE FENOTIPICAMENTE INQUADRABILI NELLA SINDROME DI CORNELIA DE LANGE. = UN CAS DE MALFORMATIONS MULTIPLES DONT LE PHENOTYPE PEUT ETRE CLASSE DANS LE SYNDROME DE CORNELIA DE LANGEGERBASI F; SCOTTO E; GIOELI R et al.SCOTTO E; 1977; PEDIATRIA; ITAL.; DA. 1977; VOL. 85; NO 1; PP. 106-117; ABS. FR. ANGL. ALLEM. ESP.; BIBL. 1 P. 1/2Article

THE DE LANGE SYNDROME IN ONE OF TWINS.CARAKUSHANSKY G; BERTHIER C.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 5; PP. 404-406; BIBL. 7 REF.Article

PRENATAL DIAGNOSIS OF RECURRENCE OF SALDINO-NOONAN DWARFISM.RICHARDSON MM; BEAUDET AL; WAGNER ML et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 3; PP. 467-471; BIBL. 10 REF.Article

A DISTINCT SKELETAL DYSPLASIA IN AN INFANT FROM CONSANGUINEOUS PARENTS.CANTU JM; MANZANO C; PAGAN P et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 139-147; BIBL. 14 REF.Article

EPIDEMIOLOGY OF CORNELIA DE LANGE'S SYNDROME.BECK B.1976; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1976; VOL. 65; NO 5; PP. 631-638; BIBL. 19 REF.Article

CAMPTOMELIC SYNDROME IN SIBLINGS.SHAFAI T; SCHWARTZ L.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 89; NO 3; PP. 512-513; BIBL. 5 REF.Article

THE CORNELIA DE LANGE SYNDROMEBOURGEOIS JM; PRUD'HOMME J; GILLEROT Y et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 3; PP. SUPPL. XI 81-88Article

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