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DEFICITS IN SPACE-FORM PERCEPTION IN PATIENTS WITH SEX CHROMOSOME MOSAICISM (45, X/46, XY)EBBIN AJ; HOWELL VV; WILSON MG et al.1980; DEVELOP. MED. CHILD NEUROL.; GBR; DA. 1980; VOL. 22; NO 3; PP. 352-361; ABS. FRE/GER/SPA; BIBL. 16 REF.Article

ADDITIONAL MANIFESTATIONS OF THE NEU-LAXOVA SYNDROMETURKEL SB; EBBIN AJ; TOWNER JW et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 227-229; BIBL. 8 REF.Article

PRIMARY HYPOPARATHYROIDISM ASSOCIATED WITH RING CHROMOSOME 18 = HYPOPARATHYROIDIE PRIMITIVE AVEC CHROMOSOME 18 EN ANNEAUOLAMBIWONNU NO; EBBIN AJ; FRASIER SD et al.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 80; NO 5; PP. 833-835; BIBL. 7 REF.Article

CHROMOSOMAL ANOMALIES IN PATIENTS WITH RETINOBLASTOMA.WILSON MG; EBBIN AJ; TOWNER JW et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 1; PP. 1-8; BIBL. 1 P.Article

FAMILIAL NEUROBLASTOMAPEGELOW CH; EBBIN AJ; POWARS D et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 5; PP. 763-765; BIBL. 15 REF.Article

PRENATAL DIAGNOSIS OF AN INHERITED TRANSLOCATION BETWEEN CHROMOSOMES NOS 9 ET 18EBBIN AJ; WILSON MG; TOWNER JW et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 65-69; BIBL. 5REF.Serial Issue

A DOUBLE ANEUPLOID MOSAIC: TRISOMY 13 AND XXY = MOSAIQUE ANEUPLOIDE DOUBLE AVEC TRISOMIE 13 ET XXYEBBIN AJ; CHU LIM R; TOWNER JW et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 365-367; BIBL. 1 REF.Serial Issue

FAMILIAL SYSTEMIC LUPUS ERYTHEMATOSUSBUCKMAN KJ; MOORE SK; EBBIN AJ et al.1978; ARCH. INTERN. MED.; USA; DA. 1978; VOL. 138; NO 11; PP. 1674-1676; BIBL. 13 REF.Article

ISOLATED GONADAL SEX CHROMOSOME MOSAICISM IN PRIMARY AMENORRHEA.FUJIMOTO A; EBBIN AJ; TOWNER JW et al.1978; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1978; VOL. 131; NO 6; PP. 699-700; BIBL. 2 REF.Article

INHERITED PARTIAL DUPLICATION OF CHROMOSOME NO 15 = DUPLICATION PARTIELLE HEREDITAIRE DU CHROMOSOME NO 15FUJIMOTO A; TOWNER JW; EBBIN AJ et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 287-291; BIBL. 9 REF.Article

GENETIC AND CLINICAL STUDIES IN 13 PATIENTS WITH THE WOLF-HIRSCHHORN SYNDROME (DEL(4P))WILSON MG; TOWNER JW; COFFIN GS et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 297-307; BIBL. 40 REF.Article

HLA PHENOTYPE FREQUENCIES IN INDIVIDUALS WITH CLEFT LIP AND/OR CLEFT PALATEBONNER SS; TERASAKI PI; THOMPSON P et al.1978; TISSUE ANTIGENS; DNK; DA. 1978; VOL. 12; NO 3; PP. 228-232; BIBL. 19 REF.Article

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