DISTAMYCIN A-DAPI BANDING OF NONFLUORESCENT Y(Y^NF) CHROMOSOMES IN 45,X/46,XY^NF MOSAICISMWISNIEWSKI LP; HIRSCHHORN K.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 130-132; BIBL. 11 REF.Article

Dominance and homozygosity in manHIRSCHHORN, K.American journal of medical genetics. 1984, Vol 18, Num 3, issn 0148-7299, 541Article

POLYGENIC INHERITANCE OF OTOSCLEROSIS.MENDLOWITZ JC; HIRSCHHORN K.1976; ANN. OTOL. RHINOL. LARYNGOL.; U.S.A.; DA. 1976; VOL. 85; NO 2; PP. 281-285; BIBL. 10 REF.Article

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

DICENTRIC Y-CHROMOSOME MOSAICISM IN A GIRL WITH CLITORAL HYPERTROPHYDE CHIERI PR; HIRSCHHORN K.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 1; PP. 149-152; BIBL. 16 REF.Article

ASPECTS RADIOLOGIQUES INHABITUELS DES DEFICITS IMMUNITAIRESROSE JS; HIRSCHHORN K; BERDON WE et al.1982; ANN. RADIOL.; ISSN 0003-4185; FRA; DA. 1982; NO 6; PP. 415-419; ABS. ENG; BIBL. 7 REF.Article

VINYL CHLORIDE EXPOSURE AND HUMAN CHROMOSOME ABERRATIONS.DUCATMAN A; HIRSCHHORN K; SELIKOFF IJ et al.1975; MUTATION RES.; NETHERL.; DA. 1975; VOL. 31; NO 3; PP. 163-168; BIBL. 17 REF.Article

SISTER-CHROMATID EXCHANGE INDUCED BY X-RAY OF HUMAN LYMPHOCYTES AND THE EFFECT OF L-CYSTEINE.ABRAMOVSKY I; VORSANGER G; HIRSCHHORN K et al.1978; MUTATION RES.; NETHERL.; DA. 1978; VOL. 50; NO 1; PP. 93-100; BIBL. 23 REF.Article

PRECISE IDENTIFICATION OF VARIOUS CHROMOSOMAL ABNORMALITIES = IDENTIFICATION PRECISE DE DIVERSES ANOMALIES CHROMOSOMIQUESHIRSCHHORN K; LUCAS M; WALLACE I et al.1973; ANN. HUM. GENET.; G.B.; DA. 1973; VOL. 36; NO 4; PP. 375-379; H.T. 4; BIBL. 12REF.Serial Issue

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

COMPLEMENT RECEPTOR IN SYNCHRONIZED CULTURES OF HUMAN HEMATOPOIETIC CELL LINESPAPENHAUSEN P; PAPAGEORGIOU P; HIRSCHHORN K et al.1975; J. IMMUNOL.; U.S.A.; DA. 1975; VOL. 114; NO 1PART. 2; PP. 519-521; BIBL. 14REF.Article

DEMONSTRATION OF HUMAN LEUKOCYTE DEGRANULATION INDUCED BY SERA FROM HOMOZYGOTES AND HETEROZYGOTES FOR CYSTIC FIBROSIS. = MISE EN EVIDENCE DE LA DEGRANULATION DES LEUCOCYTES HUMAINS PROVOQUEE PAR LE SERUM DES HOMOZYGOTES ET DES HETEROZYGOTES DE LA FIBROSE KYSTIQUECONOD EJ; CONOVER JH; HIRSCHHORN K et al.1975; PEDIATR. RES.; U.S.A.; DA. 1975; VOL. 9; NO 9; PP. 724-729; BIBL. 33 REF.Article

VINYL CHLORIDE EXPOSURE AND HUMAN CHROMOSOME ABERRATIONS.DUCATMAN A; HIRSCHHORN K; SELIKOFF IJ et al.1975; MUTATION RES.; NETHERL.; DA. 1975; VOL. 31; NO 3; PP. 163-168; BIBL. 17 REF.Article

TRISOMY 21 MOSAICISM IN A WOMAN WITH TWO CHILDREN WITH TRISOMY 21 DOWN'S SYNDROME = TRISOMIE 21 EN MOSAIQUE CHEZ UNE FEMME AYANT DEUX ENFANTS ATTEINTS D'UN SYNDROME DE DOWN AVEC TRISOMIE 21KAFFE S; HSU LYF; HIRSCHHORN K et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 378-379; BIBL. 6REF.Article

HUMAN INOSINE TRIPHOSPHATASE: CATALYTIC PROPERTIES AND POPULATION STUDIESHOLMES SL; TURNER BM; HIRSCHHORN K et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 97; NO 2-3; PP. 143-153; BIBL. 18 REF.Article

VINYL CHLORIDE EXPOSURE AND HUMAN CHROMOSOME ABERRATIONSDUCATMAN A; HIRSCHHORN K; SELIKOFF IJ et al.1975; MUTATION RES.; NETHERL.; DA. 1975; VOL. 31; NO 3; PP. 163-168; BIBL. 17 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

ASSOCIATION OF 59- AND REFRACTORY ANEMIAKAFFE S; HSU LYF; HOFFMAN R et al.1978; AMER. J. HEMATOL.; USA; DA. 1978; VOL. 4; NO 3; PP. 269-272; BIBL. 10 REF.Article

FAMILIAL TRANSLOCATION WITH PARTIAL TRISOMY OF 13 AND 22: EVIDENCE THAT SPECIFIC REGIONS OF CHROMOSOMES 13 AND 22 ARE RESPONSIBLE FOR THE PHENOTYPE OF EACH TRISOMY.KIM HJ; HSU LYF; GOLDSMITH LC et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 2; PP. 114-119; BIBL. 21 REF.Article

PRENATAL DIAGNOSIS OF TRISOMY 18. PATHOLOGIC FINDINGS IN 20-WEEK CONCEPTUS = DIAGNOSTIC ANTENATAL DE TRISOMIE 18. CONSTATATIONS ANATOMO-PATHOLOGIQUES CHEZ UN PRODUIT DE CONCEPTION DE 20SEMAINESHSU LYF; STRAUSS L; DUBIN E et al.1973; AMER. J. DIS. CHILD.; U.S.A.; DA. 1973; VOL. 125; NO 2; PP. 290-292; BIBL. 14REF.Serial Issue

RESULTS AND PITFALLS IN PRENATAL CYTOGENETIC DIAGNOSIS = RESULTATS ET PIEGES DU DIAGNOSTIC CYTOGENETIQUE ANTENATALHSU LYF; DUBIN EC; KERENYI T et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 2; PP. 112-119; BIBL. 16REF.Serial Issue

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

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