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

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AUTOSOMAL RECESSIVE SPONDYLO-EPI-METAPHYSEAL DYSPLASIA (IRAPA-TYPE) IN A MEXICAN FAMILY: DELINEATION OF THE SYNDROMEHERNANDEZ A; RAMIREZ ML; NAZARA Z et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 2; PP. 179-188; BIBL. 4 REF.Article

TYPE AND CONTRETYPE SIGNS IN MONOSOMY AND TRISOMY 9P: ON A CASE 46,XY,DEL(9) (PTER->P12:)HERNANDEZ A; RIVERA H; JIMENEZ SAINZ M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 155-157; ABS. FRE; BIBL. 13 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

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

KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY. A DISTINCT AUTOSOMAL DOMINANT GENODERMATOSISAGUIRRE NEGRETE MG; HERNANDEZ A; RAMIREZ SOLTERO S et al.1981; DERMATOLOGICA; ISSN 0011-9075; CHE; DA. 1981; VOL. 162; NO 4; PP. 300-303; BIBL. 8 REF.Article

Quiste poplíteo familiar = Kyste poplité familial = Familial popliteal cystHERNANDEZ, A; GUADALUPE AGUIRRE NEGRETE, M; NAZARA, Z et al.Revista cubana de pediatría. 1983, Vol 55, Num 3, pp 325-327, issn 0034-7531Article

Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive conditionHERNANDEZ, A; REYNOSO, M. C; SOTO, F et al.Clinical genetics. 1989, Vol 36, Num 6, pp 456-458, issn 0009-9163Article

A probably distinct autosomal recessive thoraco-limb dysplasiaRIVERA, H; PEREZ-SALAS, J. M; NAZARA, Z et al.Journal of medical genetics. 1988, Vol 25, Num 9, pp 619-622, issn 0022-2593Article

Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsHERNANDEZ, A; NAZARA, Z; REYNOSO, M. C et al.Genetic counseling. 1996, Vol 7, Num 3, pp 187-191, issn 1015-8146Article

Autosomal dominant congenital macroglossia: further delienation of the syndromeREYNOSO, M. C; HERNANDEZ, A; LIZCANO-GIL, L. A et al.Genetic counseling. 1994, Vol 5, Num 2, pp 151-154, issn 1015-8146Conference Paper

Del (8) (q212q 2200) DE NOVO in a boy without Langer-Giedion syndromeRIVERA, H; RODRIGUEZ, R. M; PLASCENCIA, M. L et al.Journal de génétique humaine. 1983, Vol 31, pp 413-418, issn 0021-7743, suppl. no 5Article

A prolable monogenic form of polyostotic fibrous dysplasiaALVAREZ-ARRATIA, M. C; RIVAS, F; AVILA-ABUNDIS, A et al.Clinical genetics. 1983, Vol 24, Num 2, pp 132-139, issn 0009-9163Article

Ehlers-Danlos features with progeroid facies and mild mental retardation. Further delineation of the syndromeHERNANDEZ, A; GUADALUPE AGUIRRE-NEGRETE, M; GONZALEZ-FLORES, S et al.Clinical genetics. 1986, Vol 30, Num 6, pp 456-461, issn 0009-9163Article

Monosomy 20p du to a de novo del(20)(p12.2): clinical and radiological delineation of the syndromeGARCIA-CRUZ, D; RIVERA, H; BARAJAS, L. O et al.Annales de génétique (Paris). 1985, Vol 28, Num 4, pp 231-234, issn 0003-3995Article

De novo dir dup(1) (q3200→4300) in an adult: further delineation of the pure 1q trisomy syndromeBARROS-NUNEZ, P; SANCHEZ-CORONA, J; ROLON, A et al.Annales de génétique (Paris). 1989, Vol 32, Num 2, pp 97-101, issn 0003-3995Article

Guadalajara camptodactyly syndrome type IICANTU, J. M; GARCIA-CRUZ, D; GIL-VIERA, J et al.Clinical genetics. 1985, Vol 28, Num 1, pp 54-60, issn 0009-9163Article