BLEPHAROCHALASIS (FUCHS) AND LAFFER-ASCHER-SYNDROM = BLEPHAROCHALASIS DE FUCHS ET SYNDROME DE LAFFER-ASCHERMUHLENDYCK H; HUNDEIKER M.1978; HAUTARZT; DEU; DA. 1978; VOL. 29; NO 9; PP. 474-477; ABS. ENG; BIBL. 20 REF.Article

TELECANTO ESTERNO SENILE ACQUISITO. SPASMO DELL' ORBICOLARE E BLEFAROFIMOSI ACQUISITA CON RILASSAMENTO DEL RAFE PALPEBRALE LATERALE, ECTROPION DELLA PALPEBRA INFERIORE ED EPIFORA = TELECANTHUS EXTERNE SENILE ACQUIS. SPASME DE L'ORBICULAIRE ET BLEPHAROPHIMOSIS ACQUIS AVEC RELACHEMENT DU RAPHE PALPEBRAL LATERAL, ECTROPION DE LA PAUPIERE INFERIEURE ET EPIPHORAACTIS G; ARAGNO M.1979; MINERVA OFTALMOL.; ITA; DA. 1979; VOL. 21; NO 3; PP. 259-261Article

Blepharophimosis and its association with female infertilityJONES, C. A; COLLIN, J. R. O.British journal of ophthalmology. 1984, Vol 68, Num 8, pp 533-534, issn 0007-1161Article

APPARENT NON-PENETRANCE FOR DYSTOPIA IN WAARDENBURG SYNDROME TYPE I, WITH SOME HINTS ON THE DIAGNOSIS OF DYSTOPIA CANTHORUM.ARIAS S; MOTA M.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 2; PP. 103-131; ABS. FRE/GER; BIBL. 25 REF.Article

SINGLE MUSCLE FIBER RECORDINGS IN THE SCHWARTZ-JAMPEL SYNDROMEJABLECKI C; SCHULTZ P.1982; MUSCLE AND NERVE; ISSN 0148-639X; USA; DA. 1982; VOL. 5; NO 9; PP. S64-S69; BIBL. 18 REF.Conference Paper

A DOMINANTLY INHERITED CONGENITAL ANOMALY SYNDROME WITH BLEPHAROPHIMOSISPUESCHEL SM; BARSEL BOWERS G.1979; J. PEDIATR.; USA; DA. 1979; VOL. 95; NO 6; PP. 1010-1012; BIBL. 6 REF.Article

OCULAR ADNEXAL PROBLEMS IN CRANIOFACIAL DEFORMITIESWHITAKER LA; KATOWITZ JA; JACOBS WE et al.1979; J. MAXILLOFACIAL SURG.; DEU; DA. 1979; VOL. 7; NO 1; PP. 55-60; BIBL. 8 REF.Article

TWO BROTHERS WITH THE MARDEN-WALKER SYNDROME: CASE REPORT AND REVIEWHOWARD FM; ROWLANDSON P.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 50-53; BIBL. 11 REF.Article

BLEPHARAPHIMOSIS-PTOSIS EPICANTHUS INVERSE. STERILITE A CYCLES LONGS ET ANOVULATOIRES. MALADIE HEREDITAIRE AUTONOME.TITECA P.1976; ; S.L.; DA. 1976; PP. (37P.); BIBL. 3 P.; (THESE DOCT. MED.; FRANCOIS RABELAIS TOURS)Thesis

W-EPICANTHOPLASTY = L'EPICANTHOPLASTIE EN WMULLIKEN JB; HOOPES JE.1975; PLAST. RECONSTR. SURG.; U.S.A.; DA. 1975; VOL. 55; NO 4; PP. 435-438; BIBL. 18 REF.Article

Two additional cases of the Ohdo blepharophimosis syndromeMAAT-KIEVIT, A; BRUNNER, H. G; MAASWINKEL-MOOIJ, P et al.American journal of medical genetics. 1993, Vol 47, Num 6, pp 901-906, issn 0148-7299Article

TIMING OF SURGERY IN CONGENITAL EYELID DEFORMITIES = DATE DE LA CHIRURGIE POUR LES MALFORMATIONS CONGENITALES DES PAUPIERESMUSTARDE JC.1974; TRANS. OPHTHALMOL. SOC. U.K.; G.B.; DA. 1974; VOL. 94; NO 1; PP. 12-18; (OPHTHALMOL. SOC. U.K. PROC. 94TH ANNU. CONGR.; 1974)Conference Paper

TRAITEMENT CHIRURGICAL DU BLEPHAROPHIMOSISROUGIER J.1973; SEM. HOP., ANN. CHIR. PLAST.; FR.; DA. 1973; VOL. 18; NO 2; PP. 141-147; ABS. ANGL.; BIBL. 5REF.Serial Issue

Blefarofimosis hereditaria con alteraciones visuales = Blepharophimosis hereditary syndrome with visual alterationRUIZ-MANJARREZ, A; GUILLEN-ANORVE, B; NUNEZ-GOMEZ, R et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1993, Vol 50, Num 8, pp 586-589, issn 0539-6115Article

Dominantly inherited syndromic blepharophimosisBIXLER, D.American journal of medical genetics. 1989, Vol 33, Num 4, issn 0148-7299, 551 [1 p.]Article

OCULAR FINDINGS IN TRIPLOIDY.FULTON AB; HOWARD RO; ALBERT DM et al.1977; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1977; VOL. 84; NO 6; PP. 859-867; BIBL. 42 REF.Article

The Ohdo blepharophimosis syndrome in a Mexican boyFIGUERA, L. E; RAMIREZ-DUENAS, M. L; RIVERA, H et al.Dysmorphology and clinical genetics. 1992, Vol 6, Num 4, pp 196-198, issn 0893-6633Article

Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23FRYNS, J. P; STRØMME, P; VAN DEN BERGHE, H et al.Clinical genetics. 1993, Vol 44, Num 3, pp 149-151, issn 0009-9163Article

LE SYNDROME DE DUBOWITZSTOLL C; LEVY JM; BUCK P et al.1980; PEDIATRIE; FRA; DA. 1980; VOL. 35; NO 2; PP. 149-152; ABS. ENG; BIBL. 5 REF.Article

BLEPHAROPHIMOSIS AND CARDIOPATHYBEAUCHAMP GR.1980; J. PEDIATR. OPHTHALMOL. STRABISMUS; ISSN 0191-3913; USA; DA. 1980; VOL. 17; NO 4; PP. 227-228; BIBL. 2 REF.Article

E.M.G. STUDIES OF TWO FAMILY CASES OF THE SCHWARTZ AND JAMPEL SYNDROME (OSTEO-CHONDRO-MUSCULAR DYSTROPHY WITH MYOTONIA). = ETUDE ELECTROMYOGRAPHIQUE DE 2 CAS FAMILIAUX DU SYNDROME DE SCHWARTZ ET JAMPEL (DYSTROPHIE OSTEO-CHONDRO-MUSCULAIRE AVEC MYOTONIECADILHAC J; BALDET P; GREZE J et al.1975; ELECTROMYOGR. CLIN. NEUROPHYSIOL.; BELG.; DA. 1975; VOL. 15; NO 1; PP. 5-12; BIBL. 15 REF.Article

A clinical and genetic study of the Say/ Barber/Biesecker/Young-Simpson type of Ohdo syndromeDAY, R; BECKETT, B; MOHAMMED, S et al.Clinical genetics. 2008, Vol 74, Num 5, pp 434-444, issn 0009-9163, 11 p.Article

Das Blepharophimose-Syndrom : Klinik un Therapie = Blepharophimosis syndromeHINTSCHICH, C. R; ZÜRCHER, M.Klinische Monatsblätter für Augenheilkunde. 1995, Vol 206, Num 3, pp 141-147, issn 0023-2165Conference Paper

One-stage correction for blepharophimosis syndromeWU, S.-Y; MA, L; TSAI, Y.-J et al.Eye (London. 1987). 2008, Vol 22, Num 3, pp 380-388, issn 0950-222X, 9 p.Article

Blepharophimosis and bilateral Duane syndrome associated with a FOXL2 mutationVINCENT, A. L; WATKINS, W. J; SLOAN, B. H et al.Clinical genetics. 2005, Vol 68, Num 6, pp 520-523, issn 0009-9163, 4 p.Article