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El cromosoma Filadelfia 30 años después = Chromosome PhiladelphiaLISKER, R.Revista de investigacion clinica. 1992, Vol 44, Num 1, pp 123-130, issn 0034-8376Article

DOUBLE BLIND STUDY OF MILK LACTOSE INTOLERANCE.LISKER R; AGUILAR L.1978; GASTROENTEROLOGY; U.S.A.; DA. 1978; VOL. 74; NO 6; PP. 1283-1285; BIBL. 13 REF.Article

MULTIPLE EPIPHYSEAL DYSPLASIA TARDA. A FAMILY WITH AUTOSOMAL RECESSIVE INHERITANCE = DYSPLASIE EPIPHYSAIRE MULTIPLE TARDIVE. UNE FAMILLE A HEREDITE AUTOSOMIQUE RECESSIVEGAMBOA I; LISKER R.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 1; PP. 15-19; BIBL. 4REF.Article

Panorama de la deficiencia de la glucosa-6-fosfato deshidrogenasa eritrocíticaLISKER, R.Revista de investigacion clinica. 1992, Vol 44, Num 2, pp 277-282, issn 0034-8376Article

INTESTINAL LACTASE DEFICIENCY AND MILK DRINKING CAPACITY IN THE ADULTLISKER R; AGUILAR L; ZAVADA C et al.1978; AMER. J. CLIN. NUTRIT.; USA; DA. 1978; VOL. 31; NO 9; PP. 1499-1503; BIBL. 15 REF.Article

RECESSIVE INHERITANCE OF THE ADULT TYPE OF INTESTINAL LACTASE DEFICIENCY.LISKER R; GONZALEZ B; DALTABUIT M et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 5; PP. 662-664; BIBL. 10 REF.Article

SERUM ATYPICAL PSEUDOCHOLINESTERASE AND LEPROSYNAVARRETE JI; LISKER R; PEREZ BRICENO R et al.1979; INTERNATION. J. DERMATOL.; USA; DA. 1979; VOL. 18; NO 10; PP. 822-823; BIBL. 6 REF.Article

BRACHYDACTYLY TYPE B AND SYMPHALANGISM IN DIFFERENT MEMBERS OF A MEXICAN FAMILYZAVALA C; HERNANDEZ ORTIZ J; LISKER R et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 131-134; ABS. FR.; BIBL. 7REF.Article

, X/47, XYY MOSAICISM IN A PATIENT WITH TURNER'S SYNDROME.LISKER R; RUZ L; MUTCHINICK O et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 2; PP. 231-233; BIBL. 10 REF.Article

UNUSUAL INHERITANCE OF BECKER TYPE MUSCULAR DYSTROPHY.AGUILAR L; LISKER R; GARCIA RAMOS G et al.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 2; PP. 116-118; BIBL. 5 REF.Article

La revisión por pares en la RIC = The peer review in our journalLORIA, A; LISKER, R.Revista de investigacion clinica. 1994, Vol 46, Num 3, pp 175-176, issn 0034-8376Article

CONSTITUTIVE HETEROCHROMATIN POLYMORPHISMS IN PATIENTS WITH MALIGNANT DISEASESAGUILAR L; LISKER R; RUZ L et al.1981; CANCER; ISSN 0008-543X; USA; DA. 1981; VOL. 47; NO 10; PP. 2437-2439; BIBL. 5 REF.Article

SYMMETRICAL REPLICATION PATTERNS AND SEX CHROMATIN BODIES FORMATION OF AN IDIC(X) (P22.3:P22.3) CHROMOSOMEMUTCHINIK O; CASAS L; RUZ L et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 3; PP. 261-264; BIBL. 15 REF.Article

DOUBLE BLIND STUDY OF MILK LACTOSE INTOLERANCE IN A GROUP OF RURAL AND URBAN CHILDRENLISKER R; AGUILAR L; LARES I et al.1980; AMER. J. CLIN. NUTRIT.; USA; DA. 1980; VOL. 33; NO 5; PP. 1049-1053; BIBL. 11 REF.Article

A NEW SYNDROME CHARACTERIZED BY MENTAL RETARDATION, EPILEPSY, PALPEBRAL CONJUNCTIVAL TELANGIECTASIAS AND IGA DEFICIENCY.AGUILAR L; LISKER R; HERNANDEZ PENICHE J et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 154-158; BIBL. 13 REF.Article

FREQUENCY OF HOMOCYSTINURIA AMONGST THE BLIND = FREQUENCE DE L'HOMOCYSTINURIE CHEZ LES AVEUGLESZAVALA C; COBO A; LISKER R et al.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 2; PP. 98-100; BIBL. 11REF.Serial Issue

FREQUENCY OF SISTER CHROMATID EXCHANGES IN SEVERE PROTEIN CALORIE MALNUTRITIONMUTCHINICK O; LISKER R; RUZ L et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 129-132; ABS. FRE; BIBL. 18 REF.Article

A CASE OF XX MALE SYNDROME = UN CAS DE SYNDROME XX MALELISKER R; FLORES F; COBO A et al.sdJ. MED. GENET.; G.B.; DA. 197; VOL. 7; NO 4; PP. 394-398; BIBL. 13REF.Serial Issue

SUPERNUMERARY BISATELLITED CHROMOSOME IN A FAMILY ASCERTAINED THROUGH A PATIENT WITH STURGE-WEBER SYNDROMEDE GUTIERREZ AC; SALAMANCA F; LISKER R et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 45-49; ABS. FR.; BIBL. 19 REF.Article

LONGITUDINAL BONE MARROW CHROMOSOME STUDIES IN POTENTIAL LEUKEMIC MYELOID DISORDERS = ETUDE LONGITUDINALE DES CHROMOSOMES DE LA MOELLE OSSEUSE DANS LES TROUBLES MYELOIDES POTENTIELLEMENT LEUCEMIQUESLISKER R; COBO DE GUTIERREZ A; VELAZQUEZ FERRARI M et al.1973; CANCER; U.S.A.; DA. 1973; VOL. 31; NO 3; PP. 509-515; BIBL. 17 REF.Serial Issue

A VARIANT GLUCOSE-6-PHOSPHATE DEHYDROGENASE GD(-) CHIAPAS. ASSOCIATED WITH MODERATE ENZYME DEFICIENCY AND OCCASIONAL HEMOLYTIC ANEMIA.LISKER R; PEREZ BRICENO R; AGRILAR L et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 1; PP. 81-84; BIBL. 10 REF.Article

ABSENCE OF CORRELATION BETWEEN Y CHROMOSOME HETEROCHROMATIN AND SEVERAL ANTHROPOMETRIC MEASUREMENTS IN A MEXICAN POPULATIONARMENDARES S; LISKER R; MUTCHINICK O et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 3; PP. 283-284; BIBL. 7 REF.Article

FREQUENCY AND TYPES OF INDUCED AND SPONTANEOUS CHROMOSOME ABERRATIONS IN RELATION TO CELL KINETICSMUTCHINICK O; RUZ L; GONSEBATT ME et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 137-140; BIBL. 26 REF.Article

PERIPHERAL MOTOR NEUROPATHY ASSOCIATED WITH AUTONOMIC DYSFUNCTION IN TWO SISTERS: NEW HEREDITARY SYNDROME.LISKER R; GARCIAS RAMOS G; DE LA ROSA LARIS C et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 255-259; BIBL. 8 REF.Article

TREATMENT OF CHRONIC PORTAL-SYSTEMIC ENCEPHALOPATHY WITH LACTOSE IN LACTASE-DEFICIENT PATIENTSURIBE M; MARQUEZ MA; GARCIA RAMOS G et al.1980; DIG. DIS. SCI.; ISSN 0163-2116; USA; DA. 1980; VOL. 25; NO 12; PP. 924-928; BIBL. 23 REF.Article

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