au.\*:("DONNELL GN")
Results 1 to 12 of 12
Selection :
DIFFERENTIAL FLUORESCENCE OF SISTER CHROMATIDS WITH 4'-6-DIAMIDINO-2-PHENYLINDOLE.LIN MS; ALFI OS; DONNELL GN et al.1976; CANAD. J. GENET. CYTOL.; CANADA; DA. 1976; VOL. 18; NO 3; PP. 545-547; ABS. FR.; BIBL. 7 REF.Article
PARTIAL TRISOMY OF THE LONG ARM OF CHROMOSOME NO7 = TRISOMIE PARTIELLE DU BRAS LONG DU CHROMOSOME NO7ALFI OS; DONNELL GN; KRAMER SL et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 2; PP. 187-189; BIBL. 4REF.Serial Issue
RADIOGRAPHIC FEATURES OF FUCOSIDOSIS.LEE FA; DONNELL GN; GWINN JL et al.1977; PEDIATR. RADIOL.; GERM.; DA. 1977; VOL. 5; NO 4; PP. 204-208; BIBL. 14 REF.Article
METABOLISM OF VALINE IN CULTURED HUMAN SKIN FIBROBLASTSOIZUMI J; NG WG; DONNELL GN et al.1979; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1979; VOL. 586; NO 1; PP. 44-54; BIBL. 15 REF.Article
MANNITOL EXCRETION IN GALACTOSEMIA PATIENTS. = EXCRETION DE MANNITOL CHEZ LES MALADES ATTEINTS DE GALACTOSEMIENG WG; DONNELL GN; BERGREN WR et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 64; NO 1; PP. 39-44; BIBL. 12 REF.Article
STUDY OF A FAMILY WITH LOS ANGELES, DUARTE, AND CLASSICAL GALACTOSEMIA VARIANTS OF GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.APPLEGARTH DA; DONNELL GN; MULLINGER M et al.1976; BIOCHEM. MED.; U.S.A.; DA. 1976; VOL. 15; NO 2; PP. 206-211; BIBL. 12 REF.Article
REGIONAL MAPPING OF THE GENE FOR HUMAN UDPGAL 4-EPIMERASE ON CHROMOSOME 1 IN MOUSE-HUMAN HYBRIDSLIN MS; OIZUMI J; NG WG et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 4; PP. 217-223; BIBL. 20 REF.Article
GALACTOKINASE-DEFICIENCY CATARACTS IN IDENTICAL TWINS = CATARACTES PAR DEFICIENCE EN GALACTO-KINASE CHEZ DES VRAIS JUMEAUXOBERMAN AE; WILSON WA; FRASIER SD et al.1972; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 74; NO 5; PP. 887-892; BIBL. 25REF.Serial Issue
THE 9P-SYNDROMEALFI OS; DONNELL GN; ALLDERDICE PW et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 11-16; ABS. FR.; BIBL. 8 REF.Article
ASSIGNMENT OF THE GENE FOR URIDINE DIPHOSPHATE GALACTOSE-4-EPIMERASE TO HUMAN CHROMOSOME 1 BY HUMAN-MOUSE SOMATIC CELL HYDRIDIZATIONLIN MS; OIZUMI J; NG WG et al.1979; SOMAT. CELL. GENET.; USA; DA. 1979; VOL. 5; NO 3; PP. 363-371; BIBL. 24 REF.Article
FRUCTOSE-INDUCED HYPERURICEMIA: OBSERVATIONS IN NORMAL CHILDREN AND IN PATIENTS WITH HEREDITARY FRUCTOSE INTOLERANCE AND GALACTOSEMIA. = HYPERURICEMIE PROVOQUEE PAR LA FRUCTOSE: OBSERVATIONS CHEZ DES ENFANTS NORMAUX ET CHEZ DES MALADES SOUFFRANT D'INTOLERANCE HEREDITAIRE AU FRUCTOSE ET DE GALACTOSEMIEKOGUT MD; ROE TF; WON NG et al.1975; PEDIATR. RES.; U.S.A.; DA. 1975; VOL. 9; NO 10; PP. 774-778; BIBL. 58 REF.Article
DELETION OF THE SHORT ARM OF CHROMOSOME #9 (46, 9P-): A NEW DELETION SYNDROMEALFI O; DONNELL GN; CRANDALL BF et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 17-22; ABS. FR.; BIBL. 19REF.Serial Issue