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kw.\*:("Campomelic dysplasia")

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Congenital bowing of the long bones: an example of a campomelic syndrome of the short-limbed normocephalic subtypeFRYNS, J. P; ANNICQ, P; ULRIX, M et al.Acta paediatrica scandinavica. 1983, Vol 72, Num 5, pp 789-791, issn 0001-656XArticle

Orthopaedic problems associated with survival in campomelic dysplasiaRAY, S; BOWEN, J. R.Clinical orthopaedics and related research. 1984, Num 185, pp 77-82, issn 0009-921XArticle

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

Campomelic Dysplasia : Echographic Suspicion in the First Trimester of Pregnancy and Final Diagnosis of Two CasesMASSARDIER, J; ROTH, P; MICHEL-CALEMARD, L et al.Fetal diagnosis and therapy. 2008, Vol 24, Num 4, pp 452-457, issn 1015-3837, 6 p.Article

La dysplasie campromélique. A propos d'une observation = Campromelic dysplasiea. Study of a caseGNAMEY, D. K; EYNARD, J.-P.Pédiatrie (Marseille). 1984, Vol 39, Num 6, pp 455-459, issn 0031-4021Article

IL NANISMO CAMPTOMELICO: A PROPOSITO DI UNA NUOVA OSSERVAZIONE = LE NANISME CAMPTOMELIQUE: A PROPOS D'UNE NOUVELLE OBSERVATIONFORMANTICI F.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 8; PP. 649-656; ABS. ENG; BIBL. 2 P.Article

Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimesterMICHEL-CALEMARD, Laurence; LESCA, Gaëtan; MOREL, Yves et al.Prenatal diagnosis. 2004, Vol 24, Num 7, pp 519-523, issn 0197-3851, 5 p.Article

Acampomelic Form of Campomelic Dysplasia with SOX9 Missense MutationGOPAKUMAR, Hariharan; SUPERTI-FURGA, Andrea; UNGER, Sheila et al.Indian journal of pediatrics. 2014, Vol 81, Num 1, pp 98-100, issn 0019-5456, 3 p.Article

New insights in congenital bowing of the femoraCORMIER-DAIRE, V; GENEVIEVE, D; MUNNICH, A et al.Clinical genetics. 2004, Vol 66, Num 3, pp 169-176, issn 0009-9163, 8 p.Article

Stüve-Wiedemann syndrome and related bent bone dysplasiasAKAWI, N. A; ALIA, B. R; AL-GAZALI, L et al.Clinical genetics. 2012, Vol 82, Num 1, pp 12-21, issn 0009-9163, 10 p.Article

THE HISTOPATHOLOGY OF CAMPTOMELIA (BENT LIMBS) A DYSCHONDROGENESISROTH SI; JIMENEZ JF; HUSTED S et al.1982; CLIN. ORTHOP. RELAT. RES.; ISSN 0009-921X; USA; DA. 1982; NO 167; PP. 152-159; BIBL. 31 REF.Article

LONG-LIMBED CAMPOMELIC DWARFISM: A RADIOLOGIC AND PATHOLOGIC STUDYAUSTIN GE; GOLD RH; MIRRA JM et al.1980; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1980; VOL. 134; NO 11; PP. 1035-1042; BIBL. 26 REF.Article

CASE REPORT 230WAGNER EJ; HANEY PJ.1983; SKELETAL RADIOLOGY; ISSN 0364-2348; DEU; DA. 1983; VOL. 9; NO 4; PP. 283-284; BIBL. 5 REF.Article

KASINSTIK KAMPOMELES SYNDROM = SYNDROME CAMPOMELIQUEPAKY F; STOEGMANN W; HOLZLEITNER P et al.1980; PAEDIATR. U. PAEDOL.; AUT; DA. 1980; VOL. 15; NO 3; PP. 245-251; ABS. ENG; BIBL. 17 REF.Article

DAS KAMPOMELE SYNDROM = LE SYNDROME CAMPOMELIQUEAMERI MR; ALEBOUYEH M; MIRFEYZ M et al.1978; MONATSSCHR. KINDERHEILKDE; DEU; DA. 1978; VOL. 126; NO 11; PP. 687-689; ABS. ENG; BIBL. 13 REF.Article

CAMPTOMELIC DWARFISM. REPORT OF CASE AND REVIEW OF THE SALIENT FEATURES.WEINER DS; BENFIELD G; ROBINSON H et al.1976; CLIN. ORTHOP. RELAT. RES.; U.S.A.; DA. 1976; NO 116; PP. 29-31; BIBL. 16 REF.Article

Un diagnostic anténatal de dysplasie campomélique = Antenatal diagnosis of campomelicREDON, J; LE GREVELLEC, J. Y; MARIE, F et al.Journal de gynécologie obstétrique et biologie de la reproduction. 1984, Vol 13, Num 4, pp 437-441, issn 0368-2315Article

CAMPOMELIELENZ W.1981; KLIN. PEDIATR.; ISSN 0300-8630; DEU; DA. 1981; VOL. 193; NO 1; PP. 10-12; ABS. ENG; BIBL. 9 REF.Article

THE CAMPOMELIC SYNDROME IN A SINGLETON AND MONOZYGOTIC TWINSMOEDJONO SJ; CRANDALL BF; SPARKES RS et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 397-401; BIBL. 16 REF.Article

LA DYSPLASIE CAMPOMELIQUE: UN CAS DE SURVIE AU-DELA DE 4 ANSNOYAL P; VERMEULIN G; HIBON D et al.1982; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1982; VOL. 39; NO 8; PP. 621-624; ABS. ENG; BIBL. 16 REF.Article

CAMPOMELIC DYSPLASIA: FURTHER ELUCIDATION OF A DISTINCT ENTITYHALL BD; SPRANGER JW.1980; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1980; VOL. 134; NO 3; PP. 285-289; BIBL. 28 REF.Article

CAMPTOMELIC SYNDROME. A RARE TYPE OF CONGENITAL DWARFISM ASSOCIATED WITH SKELETAL AND OTHER ABNORMALITIESSEGRE A; BELUFFI G; PERETTI G et al.1978; ITAL. J. ORTHOP. TRAUMATOL.; GBR; DA. 1978; VOL. 4; NO 2; PP. 237-252; BIBL. 3 P.Article

Familial Acampomelic Form of Campomelic Dysplasia Caused by a 960 kb Deletion Upstream of SOX9LECOINTRE, Claire; PICHON, Olivier; HAMEL, Antoine et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1183-1189, issn 1552-4825, 7 p.Article

Recurrent SOX9 deletion campomelic dysplasia due to somatic mosaicism in the fatherSMYK, M; OBERSZTYN, E; NOWAKOWSKA, B et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 8, pp 866-870, issn 1552-4825, 5 p.Article

Complex Genomic Rearrangement in the SOX9 5' Region in a Patient With Pierre Robin Sequence and Hypoplastic Left ScapulaFUKAMI, Maki; TSUCHIYA, Takayoshi; TAKADA, Shuji et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 7, pp 1529-1534, issn 1552-4825, 6 p.Article

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