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au.\*:("HIGGINS JV")

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MOSAICISM PRESUMABLY RELATED TO A Y/6 TRANSLOCATION IN A BOY WITH MULTIPLE CONGENITAL ABNORMALITIES.WISNIEWSKI L; HIGGINS JV.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 5; PP. 378-381; BIBL. 7 REF.Article

PARTIAL TRISOMY 2 Q AND FAMILIAL TRANSLOCATION T(2; 18) (Q 31; P 11)WISNIEWSKI L; CHAN R; HIGGINS JV et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 2; PP. 225-228; BIBL. 9 REF.Article

METABOLISM OF ALPHA-AMINOADIPIC AND ALPHA-KETOADIPIC ACIDS. STUDIES USING RAT AND BEEF LIVER, AND HUMAN LEUKOCYTES.WILSON RW; WILSON CM; HIGGINS JV et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 69; NO 2; PP. 323-332; BIBL. 16 REF.Article

PARTIAL TETRASOMY 9 IN A LIVEBORN INFANTWISNIEWSKI L; POLITIS GD; HIGGINS JV et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 147-153; BIBL. 8 REF.Article

AUTOSOMAL-RECESSIVE APLASIA CUTIS CONGENITA - REPORT OF TWO AFFECTED SIBSTORIELLO HV; HIGGINS JV; WATERMAN DF et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 153-156; BIBL. 3 REF.Article

CITRULLINEMIA. A NEW CASE, WITH IMPLICATIONS CONCERNING ADAPTATION TO DEFECTIVE UREA SYNTHESIS = CITRULLINEMIE. UN NOUVEAU CAS AVEC DES IMPLICATIONS CONCERNANT L'ADAPTATION AU DEFAUT DE SYNTHESE DE L'UREESCOTT EMUAKPOR A; HIGGINS JV; KOHRMAN AF et al.1972; PEDIATR. RES.; SWITZ.; DA. 1972; VOL. 6; NO 7; PP. 626-633; BIBL. 31 REF.Serial Issue

CYTOGENETIC AND CLINICAL STUDIES IN FIVE CASES OF INV DUP(15)WISNIEWSKI L; HASSOLD T; HEFFELFINGER J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 259-270; BIBL. 2 P.Article

THE CARRYING ANGLE IN SEX CHROMOSOME ANOMALIES = L'ANGLE CUBITO-ANTETRACHEAL DANS LES ANOMALIES DES CHROMOSOMES SEXUELSBAUGHMAN FA JR; HIGGINS JV; WADSWORTH TG et al.1974; J. AMER. MED. ASS.; U.S.A.; DA. 1974; VOL. 230; NO 5; PP. 718-720; BIBL. 18 REF.Article

CYTOGENETIC RECOGNITION OF CHROMOSOMAL DUPLICATION (DUP(1) (P31.4->P22.1)) AND THE DETECTION OF THREE DIFFERENT ALLELES AT THE PGM1 LOCUSCOUSINEAU AJ; HIGGINS JV; HACKEL E et al.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; NO 4; PP. 337-340; BIBL. 7 REF.Article

FAMILIAL OCCURENCE OF CONGENITAL PULMONARY LYMPHANGIECTASISSCOTT EMUAKPOR AB; WARREN ST; SAROJ KAPUR et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 6; PP. 532-534; BIBL. 13 REF.Article

BRIEF CLINICAL REPORT: RING-11 CHROMOSOME: PHENOTYPE-KARYOTYPE CORRELATION WITH DELETIONS OF 11QCOUSINEAU AJ; HIGGINS JV; SCOTT EMUAKPOR AB et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 29-35; BIBL. 2 P.Article

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