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au.\*:("HOO JJ")

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FAMILIAL MIDDLE LOBE BRONCHIECTASISHOO JJ.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 1; PP. 85-88; BIBL. 14 REF.Article

CLINICAL CONSEQUENCE OF XP-HOO JJ.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 349-351; BIBL. 9 REF.Article

THE AARSKOG (FACIO-DIGITO-GENITAL) SYNDROMEHOO JJ.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 4; PP. 269-276; BIBL. 9 REF.Article

A NOTE ON THE XP-HOO JJ.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 339-340; BIBL. 8 REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME 17 = TRISOMIE DU BRAS COURT DU CHROMOSOME 17LATTA E; HOO JJ.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 23; NO 3; PP. 213-217; ABS. ALLEM.; BIBL. 9REF.Article

RELATION BETWEEN THE SCE POINTS AND THE DNA REPLICATION BANDSHOO JJ; PARSLOW MI.1979; CHROMOSOMA; DEU; DA. 1979; VOL. 73; NO 1; PP. 67-74; BIBL. 14 REF.Article

A CASE OF 48, XXYY. PATERNAL ORIGIN OF THE EXTRA X CHROMOSOME = UN CAS DE 48, XXYY. ORIGINE PATERNELLE DU CHROMOSOME X SUPPLEMENTAIREHILLIG U; HOO JJ.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 2; PP. 159-161; BIBL. 8REF.Article

THE BEHAVIOR OF RING CHROMOSOME 13 = LE COMPORTEMENT DU CHROMOSOME 13 ANNULAIREHOO JJ; OBERMANN U; CRAMER H et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 3; PP. 161-171; ABS. ALLEM.; BIBL. 16REF.Article

ANTENATAL DIAGNOSIS OF MAPLE SYRUP URINE DISEASE = LE DIAGNOSTIC ANTENATAL DE LA MALADIE DE L'URINE A ODEUR DE SIROP D'ERABLEHOO JJ; LATTA E; SCHAUMLOEFFEL E et al.1974; Z. KINDERHEILKDE; DTSCH.; DA. 1974; VOL. 118; NO 3; PP. 225-229; ABS. ALLEM.; BIBL. 13REF.Article

FAMILIAL TINY 9P/20P TRANSLOCATION: 9P24 THE CRITICAL SEGMENT FOR MONOSOMY 9P SYNDROMEHOO JJ; FISCHER A; FUHRMANN W et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 4; PP. 249-252; ABS. FRE; BIBL. 11 REF.Article

PARTIAL TRISOMY 9 Q DUE TO MATERNAL 9/17 TRANSLOCATIONAFTIMOS SF; HOO JJ; PARSLOW MI et al.1980; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1980; VOL. 134; NO 9; PP. 848-850; BIBL. 13 REF.Article

A RADIOENZYMATIC ASSAY OF CATECHOL-O-METHYLTRANSFERASE IN HAIR ROOT CELLS: COMPARISON WITH ERYTHROCYTE ACTIVITYHOO JJ; STROHMEYER T; BECKERMANN WJ et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 169-171; BIBL. 16 REF.Article

DIE AKTIVITAET DES CREATINKINASE (EC 2.7.3.2)-ISOENZYMS CK-BB IM SERUM NEUGEBORENER ALS INDIKATOR EINER FRUEHKINDLICHEN SCHAEDIGUNG DES ZENTRALEN NERVENSYSTEMS = L'ACTIVITE DE L'ISOENZYME CK-BB DE LA CREATINEKINASE (EC 2.7, 3.2) DANS LE SERUM DE NOUVEAU-NES COMME INDICATEUR D'UNE LESION INFANTILE PRECOCE DU SYSTEME NERVEUX CENTRALHEINBOKEL N; HOO JJ; GOEDDE HW et al.1983; MONATSSCHRIFT FUER KINDERHEILKUNDE; ISSN 0026-9298; DEU; DA. 1983; VOL. 131; NO 5; PP. 282-285; ABS. ENG; BIBL. 18 REF.Article

TINY INTERSTITIAL DUPLICATION OF PROXIMAL 7Q IN ASSOCIATION WITH A MATERNAL PARACENTRIC INVERSIONHOO JJ; LORENZ R; FISCHER A et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 2; PP. 113-116; BIBL. 16 REF.Article

IN VITRO EFFECT OF HALOPERIDOL, CHLARPROMAZINE, IMIPRAMINE AND LITHIUM ON THE ERYTHROCYTE CATECHOL-O-METHYLTRANSFERASEHOO JJ; NOLDT P; BECKERMAN WJ et al.1982; ARZNEIM.-FARSCH.; ISSN 0004-4172; DEU; DA. 1982; VOL. 32; NO 6; PP. 681-683; ABS. GER; BIBL. 19 REF.Article

A DELETED EXTRA CHROMOSOME 22 IDENTIFIED BY DNA REPLICATION BANDINGPARSLOW M; HOO JJ; GARRY M et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 3; PP. 323-326; BIBL. 6 REF.Article

THE RING NATURE OF A TINY SUPERNUMERARY CHROMOSOME FRAGMENTHOO JJ; DRUMMOND M; PASLOW MI et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 4; PP. 331-337; BIBL. 5 REF.Article

CONFIRMATION OF REGIONAL ASSIGNMENT OF GENE FOR HUMAN ESTERASE-D TO CHROMOSOME BAND 13Q14HOO JJ; KOCH M; ZIEMSEN B et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 3; PP. 276-277; BIBL. 10 REF.Article

COMPLEX DE NOVO REARRANGEMENT OF CHROMOSOME 9 WITH CLINICAL FEATURES OF MONOSOMY 9P SYNDROMEHOO JJ; PARSLOW MI; SHAW RL et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 151-155; BIBL. 11 REF.Article

SUPERNUMERARY SMALL RING CHROMOSOME = PETIT CHROMOSOME ANNULAIRE SURNUMERAIREHOO JJ; FOERSTER C; KINDERMANN I et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 1; PP. 17-28; BIBL. 1 P. 1/2Article

CATECHOL-O-METHYLTRANSFERASE OF ERYTHROCYTES IN PATIENTS WITH ENDOGENOUS PSYCHOSESPHILIPPU G; HOO JJ; MILECH U et al.1981; PSYCHIATRY RES.; ISSN 0165-1781; NLD; DA. 1981; VOL. 4; NO 2; PP. 139-146; BIBL. 2 P.Article

MULTIPLE FEHLBILDUNGEN ALS FOLGE VON PARTIELLER TRISOMIE 4P UND PARTIELLER MONOSOMIE 18Q DURCH MEROTISCHE REKOMBINATION = MALFORMATIONS MULTIPLES DUES A UNE TRISOMIE PARTIELLE 4P ET UNE MONOSOMIE PARTIELLE 18Q RESULTANT D'UNE RECOMBINAISON MEIOTIQUEHOO JJ; FUHRMANN RIEGER A; FOERSTER W et al.1983; MONATSSCHRIFT FUER KINDERHEILKUNDE; ISSN 0026-9298; DEU; DA. 1983; VOL. 131; NO 3; PP. 169-172; ABS. ENG; BIBL. 3 REF.Article

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