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

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

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

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

AUTOSOMAL RECESSIVE MICROCEPHALY ASSOCIATED WITH CHORIORETINOPATHY.CANTU JM; ROJAS JA; GARCIA CRUZ D et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 2; PP. 243-247; BIBL. 7 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

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

GUADALAJARA CAMPTODACTYLY SYNDROME: A DISTINCT PROBABLY AUTOSOMAL RECESSIVE DISORDERCANTU JM; RIVERA H; NAZARA Z et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 3; PP. 153-159; BIBL. 14 REF.Article

TETRASOMY 9P: CLINICAL ASPECTS AND ENZYMATIC GENE DOSAGE EXPRESSIONGARCIA CRUZ D; VACA G; IBARRA B et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 4; PP. 237-242; ABS. FRE; BIBL. 12 REF.Article

A FLUORESCENT SCREENING TEST FOR RED BLOOD CELL SORBITOL DEHYDROGENASE DEFICIENCYVALA G; SANCHEZ CORONA J; GARCIA CRUZ D et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 63-64; ABS. FRE; BIBL. 10 REF.Article

RED BLOOD CELL SORBITOL DEHYDROGENASE DEFICIENCY IN A FAMILY WITH CATARACTSVACA G; IBARRA B; BRACAMONTES M et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 4; PP. 338-341; BIBL. 18 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

Inherited hypertrichosesGARCIA-CRUZ, D; FIGUERA, L. E; CANTU, J. M et al.Clinical genetics. 2002, Vol 61, Num 5, pp 321-329, issn 0009-9163Article

Condrodisplasia metafisaria tipo Schmid: aspectos clínicos, radiológicos y diagnósticos diferencial = Metaphyseal chondrodysplasia schmid type:Clinical features,radiology and differential diagnosisLIZCANO-GIL, L. A; HERNANDEZ, A; GARCIA-CRUZ, D et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1995, Vol 52, Num 5, pp 310-315, issn 0539-6115Article

Spondylo-camptodactyly syndrome : a distinct autosomal dominant entity ?LIZCANO-GIL, L. A; GARCIA-CRUZ, D; SANCHEZ-CORONA, J et al.Clinical genetics. 1995, Vol 48, Num 4, pp 173-176, issn 0009-9163Article

Unexpected familial recurrence of iris coloboma. A delayed mutation mechanism ?BARROS-NUNEZ, P; MEDINA, C; MENDOZA, R et al.Clinical genetics. 1995, Vol 48, Num 3, pp 160-161, issn 0009-9163Article

El síndrome de Robinow: aspectos clínicos y diagnóstico diferencial de una entidad con heterogeneidad genética = The Robinow syndrome:clinical features and differential diagnosis of one entity with genetic heterogeneityLIZCANO-GIL, L; GARCIA-CRUZ, D; VAZQUEZ-GARIBAY, E et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1994, Vol 51, Num 8, pp 561-564, issn 0539-6115Article

Constitutional mosaic t(2;7) (p33;p22) and other rearrangements in a girl with Wilm's tumorRIVERA, H; RUIZ, C; GARCIA-CRUZ, D et al.Annales de génétique (Paris). 1985, Vol 28, Num 1, pp 52-54, issn 0003-3995Article

G-6-PD Jalisco and G-6-PD Morelia: two new Mexican variantsVACA, G; GARCIA CRUZ, D; MEDINA, C et al.Human genetics. 1985, Vol 71, Num 1, pp 82-85, issn 0340-6717Article

A further 46,XYp-femaleRIVERA, H; MOLLER, M; BALTAZAR, L. M et al.Annales de génétique (Paris). 1988, Vol 31, Num 4, pp 244-246, issn 0003-3995Article