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2. Polydactyly in Down's syndrome. Dignan PS Am J Ment Defic; 1973 Mar; 77(5):486-91. PubMed ID: 4267396 [No Abstract] [Full Text] [Related]
3. Sibship (21q21q) translocation Down's syndrome with maternal transmission. Furbetta M; Falorni A; Antignani P; Cao A J Med Genet; 1973 Dec; 10(4):371-5. PubMed ID: 4272742 [TBL] [Abstract][Full Text] [Related]
4. Brachymesophalangia-5 without cone-epiphysis mid-5 in down's syndrome. Garn SM; Gall JC; Nagy JM Am J Phys Anthropol; 1972 Mar; 36(2):253-5. PubMed ID: 4259356 [No Abstract] [Full Text] [Related]
5. [Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21]. Mikiel-Kostyra K; Czerski P; Bartosz G; Sito A; Leyka W Pediatr Pol; 1980 Jan; 55(1):23-32. PubMed ID: 6445053 [No Abstract] [Full Text] [Related]
6. [Familial pericentric inversion of y chromosome and Down's syndrome]. García Sagredo JM; Morán Cabré A; San Román Cos-Gayón C An Esp Pediatr; 1975; 8(1):68-71. PubMed ID: 123717 [TBL] [Abstract][Full Text] [Related]
7. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes. Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425 [No Abstract] [Full Text] [Related]
8. [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; 26(2):78-81. PubMed ID: 4276194 [No Abstract] [Full Text] [Related]
9. [Skeleton of the hand in Down's syndrome]. Janovec M Acta Chir Orthop Traumatol Cech; 1971; 38(2):106-11. PubMed ID: 4255184 [No Abstract] [Full Text] [Related]
10. [Down's syndrome with G/G "tandem" translocation (author's transl)]. López Pajares I; Barreiro E; Delicado A An Esp Pediatr; 1976; 9(5):553-7. PubMed ID: 136915 [TBL] [Abstract][Full Text] [Related]
11. Study of children with Down's syndrome. Dobrzanska A Pol Med Sci Hist Bull; 1970 Jan; 13(1):8-14. PubMed ID: 4244370 [No Abstract] [Full Text] [Related]
13. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome]. Dobrzańska A; Kostrzewski J Pediatr Pol; 1970 Feb; 45(2):211-5. PubMed ID: 4245096 [No Abstract] [Full Text] [Related]
14. [Mosaicism-trisomy in fathers of two children with Down's syndrome]. Domány Z; Métneki J Acta Paediatr Acad Sci Hung; 1976; 17(3):177-81. PubMed ID: 141192 [No Abstract] [Full Text] [Related]
15. [2 children of the same mother with Down's syndrome. Cytogenetic and genealogic analysis of the family]. Kalicanin P; Marković V; Morić-Petrović S; Despotović M Srp Arh Celok Lek; 1970 May; 98(5):737-48. PubMed ID: 4253281 [No Abstract] [Full Text] [Related]
16. Familial cases of Down's syndrome a psu dic (21) (q22) and a rob (14q21q) in cousins. Matsubara T; Iinuma K; Nakagome Y; Yokochi T Jinrui Idengaku Zasshi; 1981 Mar; 26(1):55-9. PubMed ID: 6455545 [No Abstract] [Full Text] [Related]
17. [Cytogenetic and dermatoglyphic studies in Down's syndrome with G-G translocation]. Trebicka-Kwiatkowska B; Raczkiewicz B; Galińska I; Gasiorowski A Pol Tyg Lek; 1973 Aug; 28(32):1220-2. PubMed ID: 4270748 [No Abstract] [Full Text] [Related]
18. Down's syndrome 47, XX,+21 with agonadism. Maximilian C; Constantinescu-Cernea L; Brătoiu H; Filipescu G; Dumitriu L; Simionescu L; Duca D; Ioan D Endocrinologie; 1980; 18(4):289-91. PubMed ID: 6451919 [TBL] [Abstract][Full Text] [Related]
19. [Disproportion of the phalanges of hands in patients with Down's syndrome and their relatives]. Silinková-Málková E; Bĕlíkovová H Cas Lek Cesk; 1972 Jul; 111(3):728-30. PubMed ID: 4263394 [No Abstract] [Full Text] [Related]
20. Down's syndrome at young maternal age; cytogenetical and genealogical study of eighty-two families. Mikkelson M Ann Hum Genet; 1967 Aug; 31(1):51-69. PubMed ID: 4228454 [No Abstract] [Full Text] [Related] [Next] [New Search]