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3. A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations. van Hemel JO; van Biervliet JP; de Jager-van der Grift PW Clin Genet; 1975 Sep; 8(3):213-7. PubMed ID: 1175325 [No Abstract] [Full Text] [Related]
4. Cornelia de Lange syndrome in an adult male. Cherington M; Ott JE; Robinson A Neurology; 1969 Sep; 19(9):879-84. PubMed ID: 5816883 [No Abstract] [Full Text] [Related]
5. A retarded child with a 46XX,3p-q+ chromosome karyotype. Butler LJ; Hall ME; Wharton BA J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443 [No Abstract] [Full Text] [Related]
6. Cytological studies on a human ring chromosome. Cooke P; Gordon RR Ann Hum Genet; 1965 Nov; 29(2):147-50. PubMed ID: 5863838 [No Abstract] [Full Text] [Related]
7. A case with 46, XX, del (11) (q21). Faust J; Vogel W; Löning B Clin Genet; 1974; 6(2):90-7. PubMed ID: 4279151 [No Abstract] [Full Text] [Related]
8. Familial bird-headed dwarfism (Seckel's syndrome). Sauk JJ; Litt R; Espiritu CE; Delaney JR J Med Genet; 1973 Jun; 10(2):196-8. PubMed ID: 4714590 [TBL] [Abstract][Full Text] [Related]
10. Chromosomal abnormalities in a girl with physical and mental maldevelopment. Subrt I; Hníková O Hum Hered; 1970; 20(3):252-9. PubMed ID: 5489883 [No Abstract] [Full Text] [Related]
11. Ring chromosome 10:46,XX,r(10)(p15 leads to q26). Tsukino R; Tsuda N; Dezawa T; Ishii T; Koike M J Med Genet; 1980 Apr; 17(2):148-50. PubMed ID: 7381872 [TBL] [Abstract][Full Text] [Related]
12. G-group ring chromosome in a mentally subnormal girl. Richards BW; Rundle AT; Hatton WM; Stewart A J Ment Defic Res; 1971 Mar; 15(1):61-72. PubMed ID: 4253116 [No Abstract] [Full Text] [Related]
13. Aneusomy by recombination: a possible example involving the E18 chromosome. Richardson HB; Bartalos M Acta Genet Med Gemellol (Roma); 1969 Apr; 18(2):117-24. PubMed ID: 5364594 [No Abstract] [Full Text] [Related]
14. A case with short arm deletion of chromosome 18 (18p-syndrome). Kumagai M; Kikuchi Y; Oishi H; Matsuda E; Kato J Jinrui Idengaku Zasshi; 1973 Jun; 18(1):24-36. PubMed ID: 4796358 [No Abstract] [Full Text] [Related]
15. Skeletal changes in the Cornelia de Lange syndrome. Lee FA; Kenny FM Am J Roentgenol Radium Ther Nucl Med; 1967 May; 100(1):27-39. PubMed ID: 6023899 [No Abstract] [Full Text] [Related]
16. A possible case of trisomy 22. Chaudhuri A; Chandra RK; Kaul KK; Dabke AT; Chaudhuri KC J Ment Defic Res; 1968 Sep; 12(3):177-86. PubMed ID: 5722466 [No Abstract] [Full Text] [Related]
18. PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER). DYGGVE HV; MIKKELSEN M Arch Dis Child; 1965 Feb; 40(209):82-5. PubMed ID: 14259280 [No Abstract] [Full Text] [Related]
19. Ring chromosome 18 in a patient with multiple anomalies. Palmer CG; Fareed N; Merritt AD J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991 [No Abstract] [Full Text] [Related]
20. Mental retardation in a child with a long B-group chromosome. Tischler B; Corey MJ; Co-Te P J Med Genet; 1968 Jun; 5(2):134-6. PubMed ID: 5722883 [No Abstract] [Full Text] [Related] [Next] [New Search]