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2. [Down's syndrome with unusual karyotype: tandem duplication of chromosome 21]. Giuffrè L; Cammarata M; Corsello G; Pecoraro MR; Piccione M; Vitaliti SM Minerva Pediatr; 1988 May; 40(5):287-90. PubMed ID: 2971868 [No Abstract] [Full Text] [Related]
3. Translocation (14;21)(q11;q22) in a woman with history of abortions and a child with Down's syndrome. Sudha T; Gopinath PM Ann Genet; 1990; 33(3):162-4. PubMed ID: 2149630 [TBL] [Abstract][Full Text] [Related]
4. [Cytogenetic studies of families of patients with Down's syndrome]. Davidenkova EF; Kolosova NN; Pantova IG; Shushval ON Tsitologiia; 1966; 8(2):277-82. PubMed ID: 4228480 [No Abstract] [Full Text] [Related]
5. Down's syndrome and leukemia: mechanism of additional chromosomal abnormalities. Goh K; Lee H; Miller G Am J Ment Defic; 1978 May; 82(6):542-8. PubMed ID: 148844 [TBL] [Abstract][Full Text] [Related]
6. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome. Visfeldt J Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134 [No Abstract] [Full Text] [Related]
7. 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]
8. Cytogenetic studies in Down syndrome. Verma IC; Mathew S; Elango R; Shukla A Indian Pediatr; 1991 Sep; 28(9):991-6. PubMed ID: 1839389 [TBL] [Abstract][Full Text] [Related]
9. [Frequency of mixoploidy in 85 index cases with Down syndrome]. Armendares S; Buentellos L; Salamanca F Rev Invest Clin; 1990; 42(2):103-7. PubMed ID: 2148432 [TBL] [Abstract][Full Text] [Related]
10. [Unusual cases of the inheritance of Down's syndrome]. Buzhievskaia TI; Chaĭkovskaia TL; Skiban GV; Zerova-Liubimova TE; Kochubeĭ TP Tsitol Genet; 1988; 22(3):25-9. PubMed ID: 2973166 [TBL] [Abstract][Full Text] [Related]
11. Comparative analysis of the rates of chromosome damage induced by bleomycin radiomimetic in human trisomic and diploid lymphocytes: in vitro cultures from a mosaic of a Down's syndrome individual. Cano J; Caparros MM; Pretel A Cytobios; 1995; 83(334):159-66. PubMed ID: 8620688 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)]. Butomo IV; Prozorova MV; Khitrikova LE Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655 [TBL] [Abstract][Full Text] [Related]
14. Down's syndrome. I. Cytogenetics. Maximilian C; Duca D; Pop T; Toncescu N; Ioan D Endocrinologie; 1980; 18(4):273-5. PubMed ID: 6451918 [TBL] [Abstract][Full Text] [Related]
15. [A case of familial paracentric inversion associated with Down's syndrome. 47, XX, +21, inv (1) (p22p36)]. Alonso Villa MJ; Plasencia Amela A; Hernando Acero I; Benavides Benavides A; Fernández Cuesta M; Fernández Toral J An Esp Pediatr; 1990 Mar; 32(3):257-8. PubMed ID: 2140666 [No Abstract] [Full Text] [Related]
16. Karyotype variation and behavior in Down's syndrome: methodological review. Gibson D Am J Ment Defic; 1973 Sep; 78(2):128-33. PubMed ID: 4272254 [No Abstract] [Full Text] [Related]
17. [Value of chromosome studies in prevention of Down's syndrome (mongolism)]. Pullé C; Pugliatti V; Mollìca G Arch Ostet Ginecol; 1966; 71(5):461-72. PubMed ID: 4231024 [No Abstract] [Full Text] [Related]
18. [Cytogenetic study and chromosome abnormalities of Alzheimer's disease and Down's syndrome]. Asaka A Nihon Rinsho; 1988 Jul; 46(7):1502-7. PubMed ID: 2975715 [No Abstract] [Full Text] [Related]
19. Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study. Fraisse J; Philip T; Bertheas MF; Lauras B Ann Genet; 1986; 29(3):177-80. PubMed ID: 2947533 [TBL] [Abstract][Full Text] [Related]
20. Chromosome 16 heterology. Nonspecific variation in karyotype? Kelly S; Almy R N Y State J Med; 1971 Oct; 71(19):2297-9. PubMed ID: 4255306 [No Abstract] [Full Text] [Related] [Next] [New Search]