PROPERTIES OF PLACENTAL ALKALINE PHOSPHATASE. III. THERMOSTABILITY AND UREA INHIBITION OF ISOLATED COMPONENTS OF THE THREE COMMON PHENOTYPES = PROPRIETES DE LA PHOSPHATASE ALCALINE PLACENTAIRE. III. THERMOSTABILITE ET INHIBITION PAR L'UREE DES COMPOSANTES ISOLEES DES TROIS PHENOTYPES COURANTSBERATIS NG; HIRSCHHORN K.1972; BIOCHEM. GENET.; U.S.A.; DA. 1972; VOL. 6; NO 1; PP. 1-8; BIBL. 18REF.Serial Issue

ACCUMULATION OF GANGLIOSIDE G_M2 IN CEREBROSPINAL FLUID OF A PATIENT WITH THE VARIANT AB OF INFANTILE G_M2 GANGLIOSIDOSISPULLARKAT RK; REHA H; BERATIS NG et al.1981; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1981; VOL. 68; NO 1; PP. 106-108; BIBL. 7 REF.Article

CHARACTERIZATION OF THE MOLECULAR DEFECT IN INFANTILE AND ADULT ACID ALPHA -GLUCOSIDASE DEFICIENCY FIBROBLASTSBERATIS NG; LABADIE GU; HIRSCHHORN K et al.1978; J. CLIN. INVEST.; USA; DA. 1978; VOL. 62; NO 6; PP. 1264-1274; BIBL. 27 REF.Article

PROPERTIES OF PLACENTAL ALKALINE PHOSPHATASE. II. INTERACTIONS OF FAST- AND SLOW-MIGRATING COMPONENTS = PROPRIETES DE LA PHOSPHATASE ALCALINE PLACENTAIRE. II. INTERACTION ENTRE COMPOSANTS A MIGRATION RAPIDE ET LENTEBERATIS NG; SEEGERS W; HIRSCHHORN K et al.1971; BIOCHEM. GENET.; U.S.A.; DA. 1971; VOL. 5; NO 4; PP. 367-377; BIBL. 9REF.Serial Issue

ADENOSINE DEAMINASE. ALTERATIONS IN ACTIVITY AND ISOZYMES DURING GROWTH OF NORMAL AND GENETICALLY DEFICIENT FIBROBLASTSHIRSCHHORN R; BERATIS NG; MARTINIUK F et al.1978; EXPR. CELL RES.; USA; DA. 1978; VOL. 117; NO 1; PP. 103-109; BIBL. 28 REF.Article

REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE ACTIVITY AND THE ESTERIFICATION OF CHOLESTEROL IN HUMAN LONG TERM LYMPHOID CELL LINESKAYDEN HJ; HATAM L; BERATIS NG et al.1976; BIOCHEMISTRY; U.S.A.; DA. 1976; VOL. 15; NO 3; PP. 521-528; BIBL. 16 REF.Article

METHIONINE UTILIZATION IN LONG-TERM HUMAN LYMPHOID CELL LINESGUARINI L; STURMAN JA; GAULL GE et al.1981; J. CELL. PHYSIOL.; ISSN 0021-9541; USA; DA. 1981; VOL. 106; NO 3; PP. 369-374; BIBL. 18 REF.Article

PARENTAL MOSAICISM IN TRISOMY 18 = MOSAICISME PARENTAL ET TRISOMIE 18BERATIS NG; KARDON NB; HSU LYF et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 6; PP. 908-911; BIBL. 22REF.Serial Issue

STABILITY OF TRISOMIC (47, 18+) CELLS IN LONG-TERM MOSAIC SKIN FIBROBLAST CULTUREBERATIS NG; HSU LYF; KUTINSKY E et al.1972; CANAD. J. GENET. CYTOL.; CANADA; DA. 1972; VOL. 14; NO 4; PP. 869-870; BIBL. 3REF.Serial Issue

TRANSSULFURATION BY HUMAN LONG TERM LYMPHOID LINES. NORMAL AND CYSTATHIONASE-DEFICIENT CELLSSTURMAN JA; BERATIS NG; GUARINI L et al.1980; J. BIOL. CHEM.; USA; DA. 1980; VOL. 255; NO 10; PP. 4763-4765; BIBL. 14 REF.Article

⁶⁴CU METABOLISM IN MENKES AND NORMAL CULTURED SKIN FIBROBLASTS.BERATIS NG; PRICE P; LABADIE G et al.1978; PEDIATR. RES.; USA; DA. 1978; VOL. 12; NO 6; PP. 699-702; BIBL. 18 REF.Article

ALPHA -L-FUCOSIDASE IN CULTURED SKIN FIBROBLASTS FROM NORMAL SUBJECTS AND FUCOSIDOSIS PATIENTS.BERATIS NG; TURNER BM; LABADIE G et al.1977; PEDIATR. RES.; U.S.A.; DA. 1977; VOL. 11; NO 7; PP. 862-866; BIBL. 29 REF.Article

GALACTOSEMIA. REPOSITORY IDENTIFICATION NOS. GM-438 TO GM-442.KAFFE S; BERATIS NG; HIRSCHHORN K et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 1; PP. 62-64; BIBL. 3 REF.Article

FUCOSIDOSIS TYPE 2. REPOSITORY IDENTIFICATION NOS. GM-289 TO GM-292.BERATIS NG; KOUSSEFF BG; HIRSCHHORN K et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 3; PP. 195-197; BIBL. 5 REF.Article

POLYMORPHISM OF HUMAN ALPHA FUCOSIDASE.TURNER BM; TURNER VS; BERATIS NG et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 5; PP. 651-661; BIBL. 11 REF.Article

CYSTATHIONASE DEFICIENCY: THE EFFECT OF COFACTOR ON THE STABILITY OF NORMAL AND ABNORMAL ENZYME FROM LYMPHOID CELL LINESPASCAL TA; BERATIS NG; TALLAN HH et al.1979; ENZYME; CHE; DA. 1979; VOL. 24; NO 4; PP. 265-268; BIBL. 15 REF.Article

CYSTATHIONASE DEFICIENCY: EVIDENCE FOR GENETIC HETEROGENEITY IN PRIMARY CYSTATHIONINURIA.PASCAL TA; GAULL GE; BERATIS NG et al.1978; PEDIATR. RES.; U.S.A.; DA. 1978; VOL. 12; NO 2; PP. 125-133; BIBL. 44 REF.Article

MAROTEAUX-LAMY SYNDROME. REPOSITORY IDENTIFICATION NOS. GM-519, 520, 935, 942, 943 AND 1022.BERATIS NG; HIRSCHHORN K; FRIEDMAN S et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 4; PP. 236-238; BIBL. 4 REF.Article

SKELETAL ABNORMALITIES IN THE KNIEST SYNDROME WITH MUCOPOLYSACCHARIDURIABRILL PW; KIM HJ; BERATIS NG et al.1975; AMER. J. ROENTGENOL. RADIUM THERAPY NUCL. MED.; U.S.A.; DA. 1975; VOL. 125; NO 3; PP. 731-738; BIBL. 10 REF.Article

ARYLSULFATASE B DEFICIENCY IN MAROTEAUX-LAMY SYNDROME: CELLULAR STUDIES AND CARRIER IDENTIFICATION. = LE DEFICIT EN ARYLSULFATASE B DANS LE SYNDROME DE MAROTEAUX-LAMY: ETUDES CELLULAIRES ET IDENTIFICATION DES CONDUCTEURSBERATIS NG; TURNER BM; WEISS R et al.1975; PEDIATR. RES.; U.S.A.; DA. 1975; VOL. 9; NO 5; PP. 475-486; BIBL. 37 REF.Article

A DIFFERENTIAL STAINING TECHNIQUE FOR CHROMOSOME IDENTIFICATION AND ITS COMPARISON WITH FLUORESCENCE TECHNIQUE = TECHNIQUE DE COLORATION DIFFERENTIELLE POUR L'IDENTIFICATION DES CHROMOSOMES ET COMPARAISON AVEC LA TECHNIQUE PAR FLUORESCENCECHERNAY PR; KARBON NB; HSU LY et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 5; PP. 347-356; BIBL. 14 REF.Serial Issue

KNIEST SYNDROME WITH DOMINANT INHERITANCE AND MUCOPOLYSACCHARIDURIA. = SYNDROME DE KNIEST DE TYPE HEREDITAIRE DOMINANT ET MUCOPOLYSACCHARIDURIEKIM HJ; BERATIS NG; BRILL P et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 6; PP. 755-764; BIBL. 1 P.Article

FUCOSIDOSIS TYPE 2. = FUCOSIDOSE DE TYPE 2KOUSSEFF BG; BERATIS NG; STRAUSS L et al.1976; PEDIATRICS; U.S.A.; DA. 1976; VOL. 57; NO 2; PP. 205-213; BIBL. 20 REF.Article