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au.\*:("CANTU JM")

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HETEROGENIC MONOZYGOCITY: EVIDENCE FOR THE TRANSMISSION OF HALF CHROMATID MUTATIONS IN HUMANS.CANTU JM.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 2; PP. 190-191; BIBL. 9 REF.Article

PRODUCT REPLACEMENT THERAPY IN STEROID 5ALPHA -REDUCTASE DEFICIENCYCANTU JM.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 120-121; ABS. FRE; BIBL. 7 REF.Article

A ROBERTSONIAN TRANSLOCATION IN THE DOMESTIC PIG (SUS SCROFA) 37,XX,-13,-17,T ROB(13;17)ALONSO RA; CANTU JM.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 50-52; ABS. FRE; BIBL. 14 REF.Article

CONGENITAL SEVERE GENERALIZED MUSCLE HYPERTONIA DURING WAKEFULNESS. A DISTINCT AUTOSOMAL RECESSIVE DISORDER = HYPERTONIE MUSCULAIRE GENERALISEE GRAVE CONGENITALE DURANT L'ETAT DE VEILLE. UNE MALADIE AUTOSOMIQUE RECESSIVE INDIVIDUALISEECANTU JM; CUELLAR A.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 1; PP. 32-35; BIBL. 9 REF.Article

OSTEOCHONDRODYSPLASIA IRAPA TYPE: AN ETHNIC MARKER GENE IN TWO SUBCONTINENTSARIAS S; CANTU JM.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 2; PP. 251-256; BIBL. 8 REF.Article

PHOSPHOGLUCOMUTASE: EVIDENCE FOR A NEW LOCUS EXPRESSED IN HUMAN MILKCANTU JM; IBARRA B.1982; SCIENCE; ISSN 0036-8075; USA; DA. 1982; VOL. 216; NO 45-46; PP. 639-640; BIBL. 11 REF.Article

CONCORDANCE OF MARGINAL KERATODERMA OF THE PALMS AND FAVRE-RACOUCHOT DISEASE IN MZ TWINS.CANTU JM; MACOTELA RUIZ E.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 3-4; PP. 321-322; BIBL. 7 REF.Article

HETEROZYGOUS EXPRESSION IN 3-M SLENDER-BONED NANISMGARCIA CRUZ D; CANTU JM.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 221-226; BIBL. 3 REF.Article

AUTOSOMAL RECESSIVE SENSORINEURAL-CONDUCTIVE DEAFNESS, MENTAL RETARDATION, AND PINNA ANOMALIES.CANTU JM; RUENES R; GARCIA CRUZ D et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 40; NO 2; PP. 231-234; BIBL. 2 REF.Article

SILENT MICROCEPHALY: A DISTINCT AUTOSOMAL DOMINANT TRAITRAMIREZ ML; RIVAS F; CANTU JM et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 4; PP. 281-286; BIBL. 14 REF.Article

RECIPROCAL INTERACTIONS OF PROGESTERONE AND 17 ALPHA -OH-PROGESTERONE AS EXOGENOUS SUBSTRATES OF RAT ADRENAL 21-HYDROXYLASE.ORTA FLORES Z; CANTU JM; DOMINGUEZ OV et al.1976; J. STEROID BIOCHEM.; G.B.; DA. 1976; VOL. 7; NO 10; PP. 761-767; BIBL. 27 REF.Article

AUTOSOMAL RECESSIVE ONYCHOTRICHODYSPLASIA, CHRONIC NEUTROPENIA AND MILD MENTAL RETARDATIONHERNANDEZ A; OLIVARES F; CANTU JM et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 2; PP. 147-152; BIBL. 1 REF.Article

DOMINANT INHERITANCE OF HOLOPROSENCEPHALYCANTU JM; FRAGOSO R; GARCIA CRUZ D et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 215-220; BIBL. 11 REF.Article

TRISOMY 10P. A REPORT OF TWO CASES DUE TO A FAMILIAL TRANSLOCATION RCP (10; 21) (P 11; P 11)CANTU JM; SALAMANCA F; BUENTELLO L et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 5-11; ABS. FR.; BIBL. 20REF.Article

THIRD CASE OF A DISTINCT VARIANT OF THE EHLERS-DANLOS-SYNDROME (EDS)HERNANDEZ A; AGUIRRE NEGRETE MG; LIPAROLI JC et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 20; NO 3; PP. 222-224; BIBL. 1 REF.Article

SEVERE MENTAL DEFICIENCY, PROPORTIONATE DWARFISM, AND DELAYED SEXUAL MATURATION: A DISTINCT INHERITED SYNDROMECANTU JM; SANCHEZ CORONO J; GARCIA CRUZ D et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 2; PP. 231-234; BIBL. 11 REF.Article

CHROMOSOMAL INSTABILITY IN INCONTINENTIA PIGMENTICANTU JM; DEL CASTILLO V; JIMENEZ M et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 2; PP. 117-119; ABS. FR.; BIBL. 5REF.Serial Issue

AUTOSOMAL DOMINANT ACRODYSOSTOSISCANTU JM; HERNANDEZ A; PANDURO CERDA A et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 3; PP. 345-346; BIBL. 6 REF.Article

EFECTO TERATOGENICO DEL METRONIDAZOL SOBRE EL PROSENCEFALO = EFFET TERATOGENE DU METRONIDAZOLE SUR LE PROENCEPHALESANCHEZ CORONA J; GARCIA CRUZ D; CANTU JM et al.1983; GACETA MEDICA DE MEXICO; ISSN 0016-3813; MEX; DA. 1983; VOL. 119; NO 1; PP. 45-48; BIBL. 19 REF.Article

ASIAN KARYOTYPE (2N=42) IN THE BLACK RAT (RATTUS RATTUS) IN MEXICOALONSO RA; VILLAGOMEZ DAF; SANCHEZ A et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 133-135; ABS. FRE; BIBL. 9 REF.Article

FAMILIAL TRISOMY 21 AND PERICENTRIC INVERSION (9)(P11Q13)HERNANDEZ A; RIVERA H; CANTU JM et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 1; PP. 40-42; BIBL. 16 REF.Article

ON THE DELETION 4P16 WOLF-HIRSCHHORN SYNDROMERIVAS F; HERNANDEZ A; NAZARA Z et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 228-231; ABS. FRE; BIBL. 26 REF.Article

FURTHER CLINICAL AND RADIOLOGICAL FEATURES IN METAPHYSEAL CHONDRODYSPLASIA JANSEN TYPENAZARA Z; HERNANDEZ A; CORONA RIVERA E et al.1981; RADIOLOGY; ISSN 0033-8419; USA; DA. 1981; VOL. 140; NO 3; PP. 697-700; BIBL. 12 REF.Article

HB CHIAPAS ALPHA 2 114 PRO->ARG BETA 2: IDENTIFICATION BY HIGH PRESSURE LIQUID CHROMATOGRAPHYIBARRA B; FRANCO GAMBOA E; RAMIREZ ML et al.1981; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1981; VOL. 5; NO 6; PP. 605-608; BIBL. 10 REF.Article

A SYNDROME WITH MIXED DEAFNESS, MOZART EAR, MIDDLE AND INNER EAR DYSPLASIASGARCIA CRUZ D; SANCHEZ CORONA J; RUENES R et al.1980; J. LARYNGOL. OTOL.; GBR; DA. 1980; VOL. 94; NO 7; PP. 773-778; BIBL. 7 REF.Article

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