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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

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

Pure monosomy and trisomy 2q24.2→13105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generationsMOLLER, M; GARCIA-CRUZ, D; RIVERA, H et al.Human genetics. 1984, Vol 68, Num 1, pp 77-86, issn 0340-6717Article

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

PARTIAL MISPAIRING AND CROSSING-OVER BETWEEN BETA O AND DELTA GENES AS THE ORIGIN OF THE DELTA BETA O THALASSEMIA GENE. A SINGLE MUTATIONAL EVENT HYPOTHESISCANTU JM; IBARRA B; VACA G et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 191-198; BIBL. 2 P.Article

SIMULTANEOUS TRISOMY 10Q24->QTER AND MONOSOMY 4P16: AN EXAMPLE OF EPISTASIS AT THE CHROMOSOME LEVELCANTU JM; HERNANDEZ A; NAZARA Z et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 41-44; ABS. FRE; BIBL. 27 REF.Article

AUTOSOMAL RECESSIVE INHERITANCE OF ATRICHIA CONGENITACANTU JM; SANCHEZ CORONA J; GONZALEZ MENDOZA A et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 3; PP. 209-212; BIBL. 8 REF.Article

SOME CLINICAL AND CYTOGENETIC OBSERVATIONS ON A RING CHROMOSOME 13 (P11Q34)HERNANDEZ A; GARCIA CRUZ D; PLASCENCIA L et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 221-224; ABS. FRE; BIBL. 13 REF.Article

A "NEW" AUTOSOMAL DOMINANT GENODERMATOSIS CHARACTERIZED BY HYPERPIGMENTED SPOTS AND PALMOPLANTAR HYPERKERATOSESCANTU JM; SANCHEZ CORONA J; FRAGOSO R et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 165-168; BIBL. 8 REF.Article

A SIMPLE SCREENING PROCEDURE FOR ADENILATE KINASE, HEXOKINASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCIESVACA G; SANCHEZ CORONA J; OLIVARES N et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 190-192; ABS. FRE; BIBL. 6 REF.Article

PARTIAL TRISOMY 1Q AND MONOSOMY 18Q DUE TO A DE NOVO T(1;18)(Q25;Q23)SOLE MT; RIVERA H; SANCHEZ CORONA J et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 120-122; ABS. FRE; BIBL. 28 REF.Article

SIMULTANEOUS PARTIAL TRISOMY 4P AND MONOSOMY 10P RESULTING FROM A PATERNAL BALANCED TRANSLOCATIONSANCHEZ CORONA J; GARCIA CRUZ D; RIVERA H et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 41-43; ABS. FRE; BIBL. 18 REF.Article

INDIVIDUALIZATION OF A SYNDROME WITH MENTAL DEFICIENCY, MACROCRANIUM, PECULAR FACIES, AND CARDIAC AND SKELETAL ANOMALIESCANTU JM; SANCHEZ CORONA J; HERNANDES A et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 4; PP. 172-179; BIBL. 6 REF.Article

A DISTINCT OSTEOCHONDRODYSPLASIA WITH HYPERTRICHOSIS. INDIVIDUALIZATION OF A PROBABLE AUTOSOMAL RECESSIVE ENTITYCANTU JM; GARCIA CRUZ D; SANCHEZ CORONA J et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 36-41; BIBL. 4 REF.Article

SOME OBSERVATIONS ON THE MENTAL DEFICIENCY, NORMOFUNCTIONAL TESTICULAR HYPERPLASIA AND FRA(X) (Q28) CHROMOSOME SYNDROMERIVERA H; HERNANDEZ A; PLASCENCIA L et al.1981; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1981; VOL. 24; NO 4; PP. 220-222; ABS. FRE; BIBL. 37 REF.Article

3-M SLENDER-BONED NANISMCANTU JM; GARCIA CRUZ D; SANCHEZ CORONA J et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 10; PP. 905-908; BIBL. 5 REF.Article

A SCREENING TEST FOR PHOSPHOGLYCERATE KINASE DEFICIENCYVACA G; WUNSCH C; MEDINA C et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 191-192; ABS. FRE; BIBL. 12 REF.Article

A SIMPLE ASSAY FOR URIDINE DIPHOSPHATE GALACTOSE 4-EPIMERASE ACTIVITYVACA G; SANCHEZ CORONA J; OLIVARES N et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 126-128; ABS. FRE; BIBL. 10 REF.Article

LOS ANGELES VARIANT OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE (EC 2.7.7.12) IN A MEXICAN FAMILYIBARRA B; VACA G; SANCHEZ CORONA J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 121-124; BIBL. 17 REF.Article

A SIMPLE RAPID FLUORESCENT ASSAY FOR ADENOSINE DEAMINASE ACTIVITYVACA G; SANCHEZ CORONA J; OLIVARES N et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 182-184; ABS. FRE; BIBL. 10 REF.Article

FAMILIAL COMEDONES: EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCECANTU JM; GOMEZ BUSTAMENTE MO; GONZALEZ MENDOZA A et al.1978; ARCH. DERMATOL.; USA; DA. 1978; VOL. 114; NO 12; PP. 1807-1809; BIBL. 4 REF.Article

Osteopoikilosis : report of a familial case = Ostéopoecilie: à propos d'une atteinte familialeSARRALDE, A; GARCIA-CRUZ, D; NAZARA, Z et al.Genetic counseling. 1994, Vol 5, Num 4, pp 373-375, issn 1015-8146Article

Determinación cualitativa y cuantitativa de glucosaminoglucanos urinarios en pacientes con osteocondrodisplasias = Qualitative and quantitative determinations of urinary glycosaminoglycanes in patients with osteochondrodysplasiasSANCHEZ-CORONA, J; GALLEGOS-ARREOLA, M. P; CONTRERAS-SANCHEZ, O et al.Archivos de investigación medica. 1990, Vol 21, Num 4, pp 353-356, issn 0066-6769Article

De novo t(4;5) (q3100; q2200) with del (5) (q1500; q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segmentRIVERA, H; ROLON, A; SANCHEZ-CORONA, J et al.Clinical genetics. 1985, Vol 27, Num 1, pp 105-109, issn 0009-9163Article

A SIMPLE SCREENING PROCEDURE FOR GLUCOSE PHOSPHATE ISOMERASE, PHOSPHOFRUCTOKINASE, ALDOLASE AND GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE DEFICIENCIESVACA G; MEDINA C; WUNSCH C et al.1981; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1981; VOL. 24; NO 4; PP. 251-253; ABS. FRE; BIBL. 11 REF.Article

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