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Journal Abstract Search
87 related items for PubMed ID: 4248804
21. [Down's syndrome. Mongolism, trisomy 21]. Mikkelsen M, Niebuhr E, Warburg M. Ugeskr Laeger; 1971 Apr 02; 133(13):596-7. PubMed ID: 4252011 [No Abstract] [Full Text] [Related]
24. Osseous malformations associated with chromosome abnormalities. Weiss L, Reynolds WA. Orthop Clin North Am; 1972 Nov 02; 3(3):713-32. PubMed ID: 4264453 [No Abstract] [Full Text] [Related]
25. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy. Orye E, Verhaaren H. Ann Genet; 1974 Sep 02; 17(3):217-20. PubMed ID: 4141590 [No Abstract] [Full Text] [Related]
27. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant]. De Prà M, Lunetta Q. Minerva Pediatr; 1974 Jan 28; 26(2):78-81. PubMed ID: 4276194 [No Abstract] [Full Text] [Related]
28. Congenital camptodactyly associated with the 48,XXYY syndrome. Bosch AM, Hack WW, Schrander-Stumpel CT. Genet Couns; 1998 Jan 28; 9(1):19-21. PubMed ID: 9555582 [Abstract] [Full Text] [Related]
29. Unusual chromosome aberrations in 3 children with Down syndrome. Osztovics M, Tóth S, Wilhelm O. Acta Paediatr Acad Sci Hung; 1982 Jan 28; 23(3):283-9. PubMed ID: 6217717 [Abstract] [Full Text] [Related]
30. Medicine and the human chromosomes. Robinson A, Puck TT. Proc Annu Meet Am Psychopathol Assoc; 1967 Jan 28; 56():1-14. PubMed ID: 4230195 [No Abstract] [Full Text] [Related]
32. Higher incidence of small Y chromosome in humans with trisomy 21 (Down syndrome). Verma RS, Huq A, Madahar C, Qazi Q, Dosik H. Pediatr Res; 1982 Sep 28; 16(9):769-70. PubMed ID: 6215610 [Abstract] [Full Text] [Related]
33. [Chromosome aberrations in children from endangered pregnancies]. Goetz P. Cesk Pediatr; 1973 Jan 28; 28(1):12-6. PubMed ID: 4265430 [No Abstract] [Full Text] [Related]
34. [Comparative effect of maternal and paternal age on the appearance of standard trisomy G]. Ros Y. Acta Genet Med Gemellol (Roma); 1973 Jan 28; 22():27-37. PubMed ID: 4275291 [No Abstract] [Full Text] [Related]
35. Studies on sex-dimorphism of peripheral blood neutrophils in the langdon-down syndrome. Dobrzańska A, Gajewska E. Pol Med J; 1968 Jan 28; 7(5):1130-6. PubMed ID: 4238324 [No Abstract] [Full Text] [Related]
37. A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+). Yanagisawa S. Jinrui Idengaku Zasshi; 1972 Sep 17; 17(1):38-43. PubMed ID: 4265909 [No Abstract] [Full Text] [Related]
38. [Familial incidence of Down's disease]. Goetz P, Svagrová E, Seemanová E, Macek M. Cesk Pediatr; 1973 Feb 17; 28(2):81-3. PubMed ID: 4265595 [No Abstract] [Full Text] [Related]
39. A 45, X woman with a 47,XY, G+ son. Lajborek-Czyz I. Clin Genet; 1976 Feb 17; 9(2):113-6. PubMed ID: 129309 [No Abstract] [Full Text] [Related]