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2. THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME. HECHT F; BRYANT JS; GRUBER D; TOWNES PL N Engl J Med; 1964 Nov; 271():1081-6. PubMed ID: 14211000 [No Abstract] [Full Text] [Related]
3. GENETIC STUDIES AND CHROMOSOMAL ANALYSES IN FAMILIES WITH MONGOLISM (DOWN'S SYNDROME) IN MORE THAN ONE MEMBER. SOLTAN HC; WIENS RG; SERGOVICH FR Acta Genet Stat Med; 1964; 14():251-64. PubMed ID: 14220466 [No Abstract] [Full Text] [Related]
4. A D/F TRANSLOCATION IN A CASE OF REGULAR TRISOMY 21 DOWN'S SYNDROME. GRIPENBERG U; AIRAKSINEN E Cytogenetics; 1964; 3():218-27. PubMed ID: 14227326 [No Abstract] [Full Text] [Related]
5. TRIPLE CHROMOSOMAL MOSAICISM IN A JAPANESE CHILD WITH DOWN'S SYNDROME. TONOMURA A; KURITA T Acta Genet Stat Med; 1964; 14():67-75. PubMed ID: 14159882 [No Abstract] [Full Text] [Related]
6. 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]
8. Reproduction in down's syndrome (mongolism): chromosomal study of mother and normal child. Tagher P; Reisman LE Obstet Gynecol; 1966 Feb; 27(2):182-4. PubMed ID: 4222376 [No Abstract] [Full Text] [Related]
9. CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS. HAMERTON JL; GIANNELLI F; POLANI PE Cytogenetics; 1965; 4():171-85. PubMed ID: 14332559 [No Abstract] [Full Text] [Related]
10. DOWN'S SYNDROME: TRISOMY AND A DE-NOVO TRANSLOCATION IN A FAMILY. PRIEST JH; BRYANT J; MOTULSKY AG Lancet; 1963 Aug; 2(7304):411-2. PubMed ID: 14044305 [No Abstract] [Full Text] [Related]
11. MULTIPLE CHROMOSOME ABERRATIONS IN DOWN'S SYNDROME ASSOCIATED WITH TWINNING AND ACUTE GRANULOCYTIC LEUKAEMIA. KIOSSOGLOU KA; ROSENBAUM E; MITUS UJ; DAMESHEK W Lancet; 1963 Nov; 2(7314):944-5. PubMed ID: 14054455 [No Abstract] [Full Text] [Related]
12. [Oxygen consumption of leukocytes in chromosome abnormalities. (Down's syndrome, ring chromosome 21, cri-du-chat syndrome, trisomy 18 and 22)]. Heyne K Med Welt; 1980 Feb; 31(7):251-4. PubMed ID: 6445033 [No Abstract] [Full Text] [Related]
13. CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS. GIANNELLI F; HAMERTON JL; CARTER CO Cytogenetics; 1965; 4():186-92. PubMed ID: 14332560 [No Abstract] [Full Text] [Related]
14. Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome. James AE; Merz T; Janower ML; Dorst JP Clin Radiol; 1971 Oct; 22(4):417-33. PubMed ID: 4257566 [No Abstract] [Full Text] [Related]
15. A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism). WARKANY J; SOUKUP SW J Pediatr; 1963 Jun; 62():890-4. PubMed ID: 13998933 [No Abstract] [Full Text] [Related]