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au.\*:("CAGIANUT B")

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ZUR APLASIE DER SCHNERVEN. = APLASIE DU NERF OPTIQUECAGIANUT B; THEILER K.1976; ARCH. (ALBRECHT VON GRAEFES) KLIN. EXPER. OPHTHALMOL.; DTSCH.; DA. 1976; VOL. 200; NO 1; PP. 93-98; ABS. ANGL.; BIBL. 1 P. 1/2Article

DIABETES JUVENILIS, TAPETO-RETINALE DEGENERATION, NEUROGENE SCHWERHOERIGKEIT (ALSTROEM-SYNDROM), ASSOZIIERT MIT EINER KONGENITALEN DYSERYTHROPOIETISCHEN ANAEMIE TYP III. = DIABETE JUVENILE, DEGENERESCENCE TAPETORETINIENNE, SURDITE NEUROGENE (SYNDROME D'ALSTROEM) ASSOCIEES A UNE ANEMIE DYSERYTHROPOIETIQUE CONGENITALE DE TYPE IIICAGIANUT B; HOCHSTRASSER P; RHYNER K et al.1977; SCHWEIZ. MED. WSCHR.; SCHWEIZ; DA. 1977; VOL. 107; NO 13; PP. 446-450; ABS. ANGL.; BIBL. 26 REF.Article

MORT CELLULAIRE PROGRAMMEE ET DEVELOPPEMENT DE L'OEIL.CAGIANUT B; THEILER K; SARAUX H et al.1976; BULL. MEM. SOC. FR. OPHTALMOL.; FR.; DA. 1976 PARU 1977; VOL. 88; PP. 323-326Article

LES MALFORMATIONS OCULAIRES ET GENERALES DANS LES TRISOMIES CLASSIQUES. ETUDE ANATOMO-PATHOLOGIQUECAGIANUT B; MOLZ G; THEILER K et al.1972; BULL. MEM. SOC. FR. OPHTALMOL.; FR.; DA. 1972; VOL. 85; PP. 54-130 (12P.); BIBL. 3REF.Serial Issue

Hereditäre Drusen der Bruchschen Membran = Drüses héréditaires de la membrane de Bruch = Hereditary drusen of Bruch's membraneCAGIANUT, B; THEILER, K.Klinische Monatsblätter für Augenheilkunde. 1987, Vol 190, Num 1, pp 21-25, issn 0023-2165Article

LA DEGENERESCENCE RETINIENNE HEREDITAIRE: NOUVEAUX ASPECTS EXPERIMENTAUXCAGIANUT B; HUWYLER A; KUTTER M et al.1981; BULL. MEM. SOC. FR. OPHTALMOL.; ISSN 0081-1092; FRA; DA. 1981 PUBL. 1982; VOL. 93; PP. 400-404; BIBL. 8 REF.Article

DYSPLASIA OPTICO-SEPTALIS = DYSPLASIE OPTICOSEPTALECAGIANUT B; SIGG P; ISLER W et al.1980; KLIN. MONATSBL. AUGENHEILKDE; DEU; DA. 1980; VOL. 176; NO 4; PP. 699-703; ABS. ENG; BIBL. 13 REF.Conference Paper

A NEW ALLELE OF OCULAR RETARDATION: EARLY DEVELOPMENT AND MORPHOGENETIC CELL DEATH.THEILER K; VARNUM DS; NADEAU JH et al.1976; ANAT. AND EMBRYOL.; GERM.; DA. 1976; VOL. 150; NO 1; PP. 85-97; BIBL. 16 REF.Article

Studies on hereditary retinal degeneration. The rd gene in the mouseCAGIANUT, B; SANDRI, G; ZILLA, P et al.Graefe's archive for clinical and experimental ophthalmology. 1985, Vol 223, Num 1, pp 16-22, issn 0721-832XArticle

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