BEITRAG ZUR KONGENITALEN ANIRIDIE = CONTRIBUTION A L'ANIRIDIE CONGENITALEPIETRUSCHKA G.1979; FOLIA OPHTHALMOL.; DDR; DA. 1979; VOL. 4; NO 4; PP. 195-203; ABS. ENG; BIBL. 22 REF.Article

MARCHESANI SYNDROME: A CASE REPORT.AMOS D; TILZER L.1976; AMER. J. OPTOM. PHYSIOL. OPT.; U.S.A.; DA. 1976; VOL. 53; NO 11; PP. 753-754; BIBL. 4 REF.Article

Le syndrome de Weill-Marchesani: à propos d'une observation = Weill-Marchesani syndrome. Considerations on a case-reportBEBE, M.Annales de pédiatrie (Paris). 1983, Vol 30, Num 9, pp 673-677, issn 0066-2097Article

MARCHESANI'S SYNDROMESCHMIDT P; BERNTH PETERSEN P.1981; OPHTHALMOLOGICA (BASEL); ISSN 0030-3755; CHE; DA. 1981; VOL. 183; NO 2; PP. 110-113; ABS. FRE/GER; BIBL. 8 REF.Article

TREATMENT OF THE WEILL-MARCHESANI SYNDROMERITCH R; WAND M.1981; ANN. OPHTHALMOL.; ISSN 0003-4886; USA; DA. 1981; VOL. 13; NO 6; PP. 665-667; BIBL. 20 REF.Article

CONTRIBUTION A L'ETUDE DE LA BIOMETRIE OCULAIRE ET DE L'HEREDITE DU SYNDROME DE WEILL-MARCHESANI.TOUSSAINT GRIGNON M.1977; ; S.L.; DA. 1977; PP. 1-118; H.T. 5; BIBL. 6 P.; (THESE DOCT. MED.; NANCY I)Thesis

CONTRIBUTION A L'ETUDE DE LA BIOMETRIE OCULAIRE ET DE L'HEREDITE DU SYNDROME DE WEIL-MARCHESANI.CORDIER J; RASPILLER A; STEHLIN B et al.1976; BULL. MEM. SOC. FR. OPHTALMOL.; FR.; DA. 1976 PARU 1977; VOL. 88; PP. 89-96; BIBL. 13 REF.Article

Les manifestations oculaires du syndrome de Weill-Marchesani : A propos de 10 observations = Ocular manifestations of Weill-Marchesani syndrome : A review of ten casesFEKI, J; CHAABOUNI, F; FOURATI, M et al.Annales de pédiatrie (Paris). 1998, Vol 45, Num 6, pp 399-402, issn 0066-2097Article

Syndrome de WEILL MARCHESANI: étude d'un cas = The WEILL MARCHESANI syndrome: report of a caseJOUHAUD, F; AUGUSTIN, P; MALBREL, C et al.Bulletin des sociétés d'ophtalmologie de France. 1984, Num 10, pp 1107-1111, issn 0081-1270Article

Weill-Marchesani syndromeKUKARNI, M. L; VENKATAMANA, V; SURESHKUMAR, C et al.Indian pediatrics. 1995, Vol 32, Num 8, pp 923-926, issn 0019-6061Article

LE GLAUCOME SECONDAIRE DE L'ENFANTWITMER R.1980; BULL. MEM. SOC. FR. OPHTALMOL.; ISSN 0081-1092; FRA; DA. 1980 PUBL. 1981; VOL. 92; PP. 218-219Article

HEREDITE ET MALADIES DU CRISTALLINCHAINE G.1981; CLIN. OPHTALMOL.; ISSN 0009-9368; FRA; DA. 1981 PUBL. 1982; NO 4; PP. 97-107Article

LE SYNDROME DE MARCHESANI (SPHEROPHAKIE-BRACHYMORPHIE)FERRIER S; NUSSLE D; FRIEDLI B et al.1980; HELV. PAEDIATR. ACTA; CHE; DA. 1980; VOL. 35; NO 2; PP. 185-198; ABS. GER/ENG; BIBL. 16 REF.Article

Vererbbare Erkrankungen mit Linsenluxation: Klinische Aspekte = Les maladies héréditaires avec luxation du cristallin: aspects cliniques = Hereditary disorders with lensluxation: clinical aspectsKOEPP, P.Klinische Monatsblätter für Augenheilkunde. 1987, Vol 190, Num 1, pp 8-10, issn 0023-2165Article

Le syndrome de Weill Marchesani: A propos d'une observation = Weill Marchesani syndrome: a case reportEL KETTANI, A; HAMDANI, M; RAIS, L et al.Journal français d'ophtalmologie. 2001, Vol 24, Num 9, pp 944-948, issn 0181-5512Article

ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndromeDAGONEAU, Nathalie; BENOIST-LASSELIN, Catherine; CORMIER-DAIRE, Valérie et al.American journal of human genetics. 2004, Vol 75, Num 5, pp 801-806, issn 0002-9297, 6 p.Article

Airway management of a patient with Weill-Marchesani syndromeKARABIYIK, Lale.Journal of clinical anesthesia. 2003, Vol 15, Num 3, pp 214-216, issn 0952-8180, 3 p.Article

Weill-Marchesani syndrome in mother and sonYOUNG, I. D; FIELE, A. R; CASEY, T. A et al.Clinical genetics. 1986, Vol 30, Num 4, pp 475-480, issn 0009-9163Article

Median nerve compression in Weill-Marchesani syndromeLEE DELLON, A; TROJAK, J. E; ROCHMAN, G. M et al.Plastic and reconstructive surgery (1963). 1984, Vol 74, Num 1, pp 127-130, issn 0032-1052Article

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndromeFAIVRE, L; GORLIN, R. J; CORMIER-DAIRE, V et al.Journal of medical genetics. 2003, Vol 40, Num 1, pp 34-36, issn 0022-2593, 3 p.Article

Weil-Marchesani syndrome : Possible linkage of the autosomal dominant form to 15q21.1WIRTZ, M. K; SAMPLES, J. R; GODFREY, M et al.American journal of medical genetics. 1996, Vol 65, Num 1, pp 68-75, issn 0148-7299Article

Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese familyMEGARBANE, A; MUSTAPHA, M; BLEIK, J et al.Clinical genetics. 2000, Vol 58, Num 6, pp 473-478, issn 0009-9163Article