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

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

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

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

Mutations of the 5α-reductase Type 2 gene in eight Mexican patients from six different pedigrees with 5α-reductase-2 deficiencyCANTO, P; VILCHIS, F; CHAVEZ, B et al.Clinical endocrinology (Oxford. Print). 1997, Vol 46, Num 2, pp 155-160, issn 0300-0664Article

A joint international study on the epidemiology of hypospadiasKÄLLEN, B; BERTOLLINI, R; CASTILLA, E et al.Acta paediatrica Scandinavica. Supplement. 1986, Num 324, issn 0300-8843, 52 p.Serial Issue

Molecular differentiation of two different translocations producing two apparent Ph chromosomes in a patient with CMLGONSEBATT, M.-E; LISKER, R; MUTCHINICK, O et al.Cancer genetics and cytogenetics. 1991, Vol 54, Num 2, pp 247-252, issn 0165-4608Article

Genetic polymorphism of the human sex hormone-binding globulin : evidence of an isoelectric focusing variant with normal androgen-binding affinitiesLARREA, F; OLIART, R. M; GRANADOS, J et al.Journal of steroid biochemistry. 1990, Vol 36, Num 6, pp 541-548, issn 0022-4731, 8 p.Article

The cyclops and the mermaid : an epidemiological study of two types of rare malformationKÄLLEN, B; CASTILLA, E. E; LANCASTER, P. A. L et al.Journal of medical genetics. 1992, Vol 29, Num 1, pp 30-35, issn 0022-2593Article

Parental fertility and infant hypospadias : an international case-control studyKÄLLEN, B; CASTILLA, E. E; KRINGELBACH, M et al.Teratology (Philadelphia, PA). 1991, Vol 44, Num 6, pp 629-634, issn 0040-3709Article

Accidental radiation injury to the hand : Anatomical and physiological considerationsBERGER, M. E; HURTADO, R; DUNLAP, J et al.Health physics (1958). 1997, Vol 72, Num 3, pp 343-348, issn 0017-9078Article

An international collaborative study of the epidemiology of esophageal atresia or stenosisROBERT, E; MUTCHINICK, O; MASTROIACOVO, P et al.Reproductive toxicology (Elmsford, NY). 1993, Vol 7, Num 5, pp 405-421, issn 0890-6238Article

An international case-control study on hypospadias the problem with variability and the beauty of diversityKÄLLEN, B; CASTILLA, E. E; ROBERT, E et al.European journal of epidemiology. 1992, Vol 8, Num 2, pp 256-263, issn 0393-2990Article