DISTRIBUTION OF CHROMOSOME BREAKS IN MEASLES, FANCONI'S ANEMIA AND CONTROLS.VON KOSKULL H; AULA P.1977; HEREDITAS; SUEDE; DA. 1977; VOL. 87; NO 1; PP. 1-10; BIBL. 40 REF.Article

A CASE OF DELETION OF SHORT ARM OF CHROMOSOME 8.LEISTI J; AULA P.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 187-194; BIBL. 4 REF.Article

INTRAUTERINE DIAGNOSIS OF CHROMOSOME ANOMALIES. = DIAGNOSTIC INTRAUTERIN DES ANOMALIES CHROMOSOMIQUESKARJALAINEN O; AULA P.1975; ANN. CHIR. GYNAECOL. FENN.; FINL.; DA. 1975; VOL. 64; NO 3; PP. 146-151; BIBL. 24 REF.Article

DISTRIBUTION OF SPONTANEOUS CHROMOSOME BREAKS IN HUMAN CHROMOSOMESAULA P; VON KOSKULL H.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 143-148; BIBL. 17 REF.Article

DECREASE IN GAMMA-GLUTAMYL TRANSPEPTIDASE ACTIVITY IN EARLY AMNIOTIC FLUID IN FETAL TRISOMY 18 SYNDROMEJALANKO H; AULA P.1982; BR. MED. J.; ISSN 0007-1447; GBR; DA. 1982; VOL. 284; NO 6329; PP. 1593-1594; BIBL. 4 REF.Article

PARTIAL TRISOMY 1(Q42->TER)LEISTI J; AULA P.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 5; PP. 371-378; BIBL. 8 REF.Article

CRY ANALYSIS OF INFANTS WITH KARYOTYPE ABNORMALITYMICHELSSON K; TUPPURAINEN N; AULA P et al.1980; NEUROPEDIATRICS; ISSN 0174-304X; DEU; DA. 1980; VOL. 11; NO 4; PP. 365-376; BIBL. 17 REF.Article

FETAL GONADAL HISTOLOGY IN XXXXY, XYY AND XXX SYNDROMESAUTIO HARMAINEN H; RAPOLA J; AULA P et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 1; PP. 1-5; BIBL. 11 REF.Article

VARIATION OF URINARY EXCRETION OF ASPARTYLGLUCOSAMINE AND ASSOCIATED CLINICAL FINDINGS IN ASPARTYLGLUCOSAMINURIAAULA P; RAIVIO KO; MAURY P et al.1980; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1980; VOL. 3; NO 4; PP. 159-162; BIBL. 17 REF.Article

ENZYME DEFECT IN SACCHAROPINURIA = DEFICIT ENZYMATIQUE DANS LA SACCHAROPINURIESIMELL O; JOHANSSON T; AULA P et al.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 1; PP. 54-57; BIBL. 16REF.Serial Issue

ENZYMATIC DIAGNOSIS AND CARRIER DETECTION OF ASPARTYLGLUCOSAMINURIA USING BLOOD SAMPLES.AULA P; RAIVIO K; AUTIO S et al.1976; PEDIATR. RES.; U.S.A.; DA. 1976; VOL. 10; NO 6; PP. 625-629; BIBL. 22 REF.Article

STRUCTURE OF TWO GLYCOASPARAGINES ISOLATED FROM THE URINE OF PATIENTS WITH ASPARTYLGLYCOSYLAMINURIA (AGU).SUGAHARA K; AKASAKI M; FUNAKOSHI I et al.1977; J. BIOCHEM.; JAP.; DA. 1977; VOL. 82; NO 5; PP. 1499-1501; BIBL. 12 REF.Article

CHARACTERIZATION OF ONE NEUTRAL AND TWO ACIDIC GLYCOASPARAGINES ISOLATED FROM THE URINE OF PATIENTS WITH ASPARTYLCOSYLAMINURIA (AGU).SUGAHARA K; FUNAKOSHI S; FUNAKOSHI I et al.1976; J. BIOCHEM.; JAP.; DA. 1976; VOL. 80; NO 2; PP. 195-201; BIBL. 21 REF.Article

PRENATAL DIAGNOSIS AND FETAL PATHOLOGY OF I-CELL DISEASE (MUCOLIPIDOSIS TYPE II). = DIAGNOSTIC ANTENATAL ET PATHOLOGIE FOETALE DE LA MALADIE A CELLULES I OU MUCOLIPIDOSE DE TYPE IIAULA P; RAPOLA J; AUTIO S et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 2; PP. 221-226; BIBL. 15 REF.Article

PREGNANCY-SPECIFIC B-1-GLYCOPROTEIN (SP₁) IN CULTURED AMNIOTIC FLUID CELLSHEIKINHEIMO M; WAHLSTROM T; AULA P et al.1980; J. CLIN. ENDOCRINOL. METAB.; ISSN 0021-972X; USA; DA. 1980; VOL. 51; NO 6; PP. 1432-1436; BIBL. 15 REF.Article

CULTURED HUMAN AMNIOTIC FLUID CELLS CHARACTERIZED WITH ANTIBODIES AGAINST INTERMEDIATE FILAMENTS IN INDIRECT IMMUNOFLUORESCENCE MICROSCOPYVIRTANEN I; VON KOSKULL H; LEHTO VP et al.1981; J. CLIN. INVEST.; ISSN 0021-9738; USA; DA. 1981; VOL. 68; NO 5; PP. 1348-1355; BIBL. 40 REF.Article

SAFETY AND ACCURACY OF MIDTRIMESTER AMNIOCENTESIS FOR PRENATAL DIAGNOSIS OF GENETIC DISORDERSAULA P; KARJALAINEN O; TERAMO K et al.1979; ANN. CLIN. RES.; FIN; DA. 1979; VOL. 11; NO 4; PP. 156-163; BIBL. 22 REF.Article

PRENATAL DIAGNOSIS OF THE MECKEL SYNDROME.AULA P; KARJALAINEN O; RAPOLA J et al.1977; AMER. J. OBSTETR. GYNECOL.; U.S.A.; DA. 1977; VOL. 129; NO 6; PP. 700-702; BIBL. 15 REF.Article

ENZYMATIC DETERMINATION OF URINARY ASPARTYLGLYCOSYLAMINE: A RAPID AND SENSITIVE METHOD TO DETECT ASPARTYLCLYCOSYLAMINURIA (AGU).SUGAHARA K; NISHIMURA K; AULA P et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 72; NO 2; PP. 265-267; BIBL. 7 REF.Article

A DELETION IN CHROMOSOME 22 CAN CAUSE DIGEORGE SYNDROMEDE LA CHAPELLE A; HERVA R; KOIVISTO M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 3; PP. 253-256; BIBL. 20 REF.Article

INCOMPLETE PRENATAL DIAGNOSIS OF G-TRISOMY MOSAICISM.SIMOLA K; AULA P; RYYNANEN M et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 6; PP. 500-503; BIBL. 11 REF.Article

CHARACTERIZATION OF A MANNOSE-CONTAINING GLYCOASPARAGINE ISOLATED FROM URINE OF A PATIENT WITH ASPARTYLGLYCOSYLAMINURIA (AGU).AKASAKI M; SUGAHARA K; FUNAKOSHI I et al.1976; F.E.B.S. LETTERS; NETHERL.; DA. 1976; VOL. 69; NO 1; PP. 191-194; BIBL. 19 REF.Article

LYMPHOCYTIC INCLUSIONS IN I-CELL DISEASE = LES INCLUSIONS LYMPHOCYTAIRES DANS LA MALADIE A CELLULES IRAPOLA J; AUTIO S; AULA P et al.1974; J. PEDIATR.; U.S.A.; DA. 1974; VOL. 85; NO 1; PP. 88-90; BIBL. 11REF.Article

SALLA DISEASE: A NEW LYSOSOMAL STORAGE DISORDER WITH DISTURBED SIALIC ACID METABOLISMRENLUND M; AULA P; RAIVIO KO et al.1983; NEUROLOGY; ISSN 0028-3878; USA; DA. 1983; VOL. 33; NO 1; PP. 57-66; BIBL. 30 REF.Article

CHARACTERIZATION OF STORAGE MATERIAL IN CULTURED FIBROBLASTS BY SPECIFIC LECTIN BINDING IN LYSOSOMAL STORAGE DISEASESVIRTANEN I; EKBLOM P; LAURILA P et al.1980; PEDIATR. RES.; ISSN 0031-3998; USA; DA. 1980; VOL. 14; NO 11; PP. 1199-1203; BIBL. 37 REF.Article