CETOACIDOSIS DIABETICA EN EL NINO Y EL ADOLESCENTE. ANALISIS DE 100 CRISIS. = CETO ACIDOSE DIABETIQUE CHEZ L'ENFANT ET L'ADOLESCENT. ANALYSE DE 100 CRISESMARTINEZ Y MARTINEZ R; MACIAS GOMEZ J; GARCIA GUERRA I et al.1976; REV. MED.; MEX.; DA. 1976; VOL. 15; NO 1; PP. 33-43; ABS. ANGL.; BIBL. 27 REF.Article

MALFORMED GENITALIA IN THE 47,XYY GENOTYPERIVERA H; HERNANDEZ A; MARTINEZ Y MARTINEZ R et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 225-227; ABS. FRE; BIBL. 20 REF.Article

The 22q distal trisomy syndrome in a recombinant childRIVERA, H; GARCIA, G; MARTINEZ Y MARTINEZ, R et al.Annales de génétique (Paris). 1988, Vol 31, Num 1, pp 47-49, issn 0003-3995Article

Autosomal dominant macroglossia: an addendum to the etiological classificationMARTINEZ Y MARTINEZ, R; REYNOSO, M. C; HERNANDEZ, A et al.Ear, nose & throat journal. 1995, Vol 74, Num 2, pp 108-109, issn 0145-5613Article

Aracnodactilia contractural congénita. Informe de dos casos clinicos = Arachnodactylie rétractile congénitale. Présentation de 2 cas cliniques = Congenital contractural arachnodactyly. Report of 2 additional casesMARTINEZ Y MARTINEZ, R; PEREZ-GARCIA, G; ARREOLA-LIZARRAGA, R et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1989, Vol 46, Num 2, pp 130-132, issn 0539-6115Article

Escasez cargenita sindromatica de los conductos biliares intrahepaticos: sindrome de Alagille. Informe de dos pacientes tratados con colestiramina = Syndromes de déficit congénital des canaux biliaires intrahépatiques. Observation de 2 cas traités par résines de cholestyramine = Syndromic congenital deficiency of intrahepatic biliary ducts. Report of 2 patients treated with cholestyramine resinMARTINEZ Y MARTINEZ, R; ESPINOZA MORA, L; GONZALEZ MENDOZA, A et al.Revista medica (Mexico). 1986, Vol 24, Num 4, pp 265-272, issn 0484-7849Article

Correlación cariotipo-fenotipo en un niño con un idic (Yp) = Correlation caryotype-phenotype chez un enfant = Karyotype-phenotype correlation in an child with idic (Yp)ALVAREZ-MOYA, C; GONZALEZ, R. M; MARTINEZ Y MARTINEZ, R et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1989, Vol 46, Num 6, pp 414-416, issn 0539-6115Article

De novo inv(5)(p15q22), del(5)(p15) in a boy with cri du chat syndromeRIVERA, H; VELAZQUEZ, R; GARCIA-ESQUIVEL, L et al.Journal of medical genetics. 1987, Vol 24, Num 3, issn 0022-2593, 186Article

The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidismMARTINEZ Y MARTINEZ, R; OCAMPO-CAMPOS, R; PEREZ-ARROYO, R et al.European journal of pediatrics. 1985, Vol 143, Num 3, pp 233-235, issn 0340-6199Article

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