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4. Banding patterns of metaphase chromosomes in Down's syndrome. Baikie AG Lancet; 1971 Aug; 2(7722):494. PubMed ID: 4105360 [No Abstract] [Full Text] [Related]
5. Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence. O'Riordan ML; Robinson JA; Buckton KE; Evans HJ Nature; 1971 Mar; 230(5290):167-8. PubMed ID: 4100531 [No Abstract] [Full Text] [Related]
6. A case of 48,XXY,21+ in an infant with Down's syndrome. Neu RL; Scheuer AQ; Gardner LI J Med Genet; 1971 Dec; 8(4):533-5. PubMed ID: 4260531 [No Abstract] [Full Text] [Related]
7. Identification of a C6-G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus. Borgaonkar DS; Bias WB; Chase GA; Sadasivan G; Herr HM; Golomb HM; Bahr GF; Kunkel LM Clin Genet; 1973; 4(1):53-7. PubMed ID: 4120631 [No Abstract] [Full Text] [Related]
8. Letter: Mongolism by tertiary trisomy. Chaganti RS; Morillo-Cucci G; Degnan M; German J Lancet; 1975 Mar; 1(7908):698-9. PubMed ID: 47133 [No Abstract] [Full Text] [Related]
9. [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]
11. 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]
12. Constitutive heterochromatin patterns of G-group chromosomes in Down's syndrome. Pathak S; Sinha AK Humangenetik; 1972; 14(4):327-9. PubMed ID: 4262184 [No Abstract] [Full Text] [Related]
13. [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]
14. Meiosis and spermatogenesis in two postpubertal males with Down's syndrome: 47, XY, G+. Kjessler B; De la Chapelle A Clin Genet; 1971; 2(1):50-7. PubMed ID: 4255785 [No Abstract] [Full Text] [Related]
15. Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation. Taysi K; Sparkes RS; O'Brien TJ; Dengler DR J Med Genet; 1982 Apr; 19(2):144-8. PubMed ID: 6210775 [TBL] [Abstract][Full Text] [Related]
16. [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]