Clinical aspects of Down syndrome from infancy to adulthoodPUESCHEL, S. M.American journal of medical genetics. Supplement. 1990, Num 7, pp 52-56, issn 1040-3787, 5 p.Article

Decreased level of T cell receptor expression by Down syndrome (trisomy 21) thymocytesMURPHY, M; LEMPERT, M. J; EPSTEIN, L. B et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 234-237, issn 1040-3787, 4 p.Article

Down syndrome children often have brain with maturation delay, retardation of growth, and cortical dysgenesisWISNIEWSKI, K. E.American journal of medical genetics. Supplement. 1990, Num 7, pp 274-281, issn 1040-3787, 8 p.Article

First trimester maternal serum α-fetoprotein screening for Down syndrome and other aneuploidiesWENGER, D; MINY, P; HOLZGREVE, W et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 89-90, issn 1040-3787, 2 p.Article

Reflections on the pathogenesis of Down syndromeOPITZ, J. M; GILBERT-BARNESS, E. F.American journal of medical genetics. Supplement. 1990, Num 7, pp 38-51, issn 1040-3787, 14 p.Article

Relationship of autoimmunity to thyroid dysfunction in children and adults with Down syndromeZORI, R. T; SCHATZ, D. A; OSTRER, H et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 238-241, issn 1040-3787, 4 p.Article

The consequences of chromosome imbalanceEPSTEIN, C. J.American journal of medical genetics. Supplement. 1990, Num 7, pp 31-37, issn 1040-3787, 7 p.Article

Thyroid function in patients with Down syndrome: preliminary results from non-institutionalized patients in the Veneto regionPOZZAN, G. B; RIGON, F; GIRELLI, M. E et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 57-58, issn 1040-3787, 2 p.Article

Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risksSACHS, E. S; JAHODA, M. G. J; LOS, F. J et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 186-188, issn 1040-3787, 3 p.Article

Heterogeneity and variability in the oral-facial-digital syndromesTORIELLO, H. V.American journal of medical genetics. Supplement. 1988, Num 4, pp 149-159, issn 1040-3787Article

Taurodontism: an anomaly of teeth reflecting disruptive developmental homeostasisWITKOP, C. J. JR; KEENAN, K. M; CERVENKA, J et al.American journal of medical genetics. Supplement. 1988, Num 4, pp 85-97, issn 1040-3787Article

Apparent Prader-Willi phenotype in a woman with ring chromosome 9HESS, R. O; MEISNER, L. F.American journal of medical genetics. Supplement. 1987, Num 3, pp 133-138, issn 1040-3787Article

Berry aneurysms, cirrhosis, pulmonary emphysema, and bilateral symmetrical cerebral calcifications: a new syndromeKAHN, E; MARKOWITZ, J; DUFFY, L et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 343-356, issn 1040-3787Article

Brief clinical report: newborn infant with del(9)(pter→q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary earsKARGAS, S. A; KARGAS, G. A; CHANDRA, S et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 161-166, issn 1040-3787Article

Demonstration of myenteric plexus abnormalities in genetic diseases by a microdissection technique: preliminary studiesGALVIS, D. A; NAKAZATO, Y; WELLS, T. R et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 329-342, issn 1040-3787Article

Electron microscopy in the diagnosis of lysosomal storage diseasesVOGLER, C; ROSENBERG, H. S; WILLIAMS, J. C et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 243-255, issn 1040-3787Article

Geleophysic dysplasia ― acromicric dysplasia with evidence of glycoprotein storageLIPSON, A. H; KAN, A. E; KOZLOWSKI, K et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 181-189, issn 1040-3787Article

Three conditions in neonatal asphyxiating thoracic dysplasia (Jeune) and short rib-polydactyly syndrome spectrum: a clinicopathologic studyYANG, S. S; LANGER, L. O. JR; CACCIARELLI, A et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 191-207, issn 1040-3787Article

Las bases de datos en la edición electrónica = Les bases de données pour l'édition électroniqueBERENGUER, J. M.1984, Num 143, pp 63-69, issn 0300-3787Article

Chromosome fragile sites in Down syndrome patientsTEDESCHI, B; VERNOLE, P; CAPOROSSI, D et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 192-194, issn 1040-3787, 3 p.Article

Distribution of X-ray-induced chromosome breakpoints in Down syndrome lymphocytesSHAFIK, H. M; AU, W. W; WHORTON, E. B et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 195-200, issn 1040-3787, 6 p.Article

Down syndrome: toward a molecular definition of the phenotypeKORENBERG, J. R; KAWASHIMA, H; M.-PULST, S et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 91-97, issn 1040-3787, 7 p.Article

ETS family of genes in leukemia and Down syndromePAPAS, T. S; WATSON, D. K; SCHWEINFEST, C. W et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 251-261, issn 1040-3787, 11 p.Article

Adults with Williams syndromeMORRIS, C. A; LEONARD, C. O; DILTS, C et al.American journal of medical genetics. Supplement. 1990, Num 6, pp 102-107, issn 1040-3787, 6 p.Article

Morphological and immunohistochemical study of Down syndrome thymusLARROCA, L. M; LAURIOLA, L; RANELLETTI, F. O et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 225-230, issn 1040-3787, 6 p.Article