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TIME OF FIRST-GENERATION METAPHASES. I: THE EFFECT OF VARIOUS CULTURE MEDIA AND OF FETAL CALF SERUM IN HUMAN LYMPHOCYTE CULTURESMUTCHINICK O; RUZ L; CASAS L et al.1980; MUTATION RES.; NLD; DA. 1980; VOL. 72; NO 1; PP. 127-134; BIBL. 17 REF.Article

PARTIAL TRISOMIES 13 AND 22 DUE TO NONDISJUNCTION OF A MATERNAL RECIPROQUAL TRANSLOCATION, T(13;22) (Q22;Q11)MUTCHINICK O; RUZ L; JIMENEZ R et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 1; PP. 89-95; BIBL. 15 REF.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

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

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

PATIENT WITH CHRONIC MYELOGENOUS LEUKEMIA AND LATE APPEARING PHILADELPHIA CHROMOSOMELISKER R; CASAS L; MUTCHINICK O et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 6; NO 3; PP. 275-277; BIBL. 7 REF.Article

Programa mexicano de Registro y Vigilancia Epidemiologica de Malformaciones Congenitas ExternasMUTCHINICK, O; LISKER, R; BABINSKI, V et al.SALUD PUBLICA DE MEXICO. 1988, Vol 30, Num 1, pp 88-100Article

GERODERMIA OSTEODYSPLASTICA HEREDITARIA: REPORT OF THREE AFFECTED BROTHERS AND LITERATURE REVIEWLISKER R; HERNANDEZ A; MARTINEZ LAVIN M et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 4; PP. 389-395; BIBL. 8 REF.Article

Riesgo para síndrome de Down por bienios y quinquenios de edad materna en la población mexicanaMUTCHINICK, O; LISKER, R; BABINSKY, V et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1991, Vol 48, Num 8, pp 534-537, issn 0539-6115Article

Programa mexicano de Registro y Vigilancia Epidemiologica de Malformaciones Congenitas ExternasMUTCHINICK, O; LISKER, R; BABINSKI, V et al.SALUD PUBLICA DE MEXICO. 1988, Vol 30, Num 1, pp 88-100Article

SISTER-CHROMATID EXCHANGES AND CELL KINETICS IN HUMAN AND RABBIT LYMPHOCYTES EXPOSED IN VIVO AND IN VITRO TO 2-BROMO-ALPHA -ERGOCRYPTINE = ECHANGES CHROMATIDES-SOEURS ET CINETIQUES CELLULAIRES, CHEZ LES LYMPHOCYTES D'HOMMES ET DE LAPINS EXPOSES A LA 2-BROMO-ALPHA ERGOCRYPTINE IN VIVO ET IN VITROMUTCHINICK O; GONSEBATT ME; RUZ L et al.1983; MUTATION RESEARCH; ISSN 0027-5107; NLD; DA. 1983; VOL. 117; NO 1-2; PP. 163-171; BIBL. 17 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

CYTOGENETIC AND ENDOCRINE STUDIES IN A 45, X FEMALE SUBJECT WITH SPONTANEOUS SEXUAL DEVELOPMENTLISKER R; JIMENEZ R; LARREA F et al.1979; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1979; VOL. 133; NO 2; PP. 149-153; BIBL. 21 REF.Article

DISTRIBUTION OF ABO BLOOD GROUPS AND OTHER GENETIC MARKERS IN MOTHERS OF INFANTS WITH CONGENITAL MALFORMATIONSLISKER R; MUTCHINICK O; PEREZ BRICENO R et al.1982; HUM. HERED.; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 3; PP. 166-169; BIBL. 5 REF.Article

Polimorfismos de los cromosomas 1, 9 y 16 en mestizos mexicanos = Polymorphisms of chromosomes 1-9-16 in mexican mixed raceARMENDARES, S; BUENTELLO, L; GAONA, O et al.Revista de investigacion clinica. 1993, Vol 45, Num 2, pp 149-153, issn 0034-8376Article

CLINICAL AND ENDOCRINE SPECTRUM IN PATIENTS WITH THE 45,X/46,XY KARYOTYPEKOFMAN S; PEREZ PALACIOS G; MEDINA M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 373-376; BIBL. 13 REF.Article

Combined trisomy 9 and Ullrich Turner syndrome in a girl with a 46,X, der(9)t(X;9)(q12;q32) karyotypeCANUN, S; MUTCHINICK, O; SHAFFER, L. G et al.American journal of medical genetics. 1998, Vol 80, Num 3, pp 199-203, issn 0148-7299Article

Mesotelioma pleural maligno familiar. Informe de tres casos = Mésothéliome pleural malin familial. Présentation de 3 cas = Malignant familial pleural mesotheliomaMUNOZ, L; GUZMAN, J; PONCE DE LEON, S et al.Revista de investigacion clinica. 1988, Vol 40, Num 4, pp 413-417, issn 0034-8376Article

Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D17S379 lociMUTCHINICK, O. M; SHAFFER, L. G; KASHORK, C. D et al.American journal of medical genetics. 1999, Vol 85, Num 2, pp 99-104, issn 0148-7299Article

Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generationsMUTCHINICK, O; RAMOS, Z; SANCHEZ, F et al.American journal of medical genetics. 1988, Vol 29, Num 1, pp 187-192, issn 0148-7299Article

Endocrine evaluation in a patient with MURCS association and ovarian agenesisMENDEZ, J. P; ULLOA-AGUIRRE, A; JANVIER SANCHEZ, F et al.European journal of obstetrics, gynecology, and reproductive biology. 1986, Vol 22, Num 3, pp 161-169, issn 0301-2115Article

Type A2 brachydactyly associated to zygodactyly in several members of a Mexican familyLISKER, R; MUTCHINICK, O; SANTOS, M. A et al.Annales de génétique (Paris). 1983, Vol 26, Num 3, pp 177-179, issn 0003-3995Article

Fetal mortality in sibships with one or more affected members with oral cleftsMUTCHINICK, O; LISKER, R; BABINSKY, V et al.American journal of medical genetics. 1985, Vol 20, Num 2, pp 317-323, issn 0148-7299Article

Cáncer gástrico familiar = Cancer gastrique familial = Familial gastric cancerLIRA PEDRIN, M. A; RAMIREZ, A; LISKER, R et al.Revista de investigacion clinica. 1987, Vol 39, Num 4, pp 359-362, issn 0034-8376Article

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