These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
133 related articles for article (PubMed ID: 5782821)
21. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl. Jacobsen P; Mikkelsen M; Rosleff F Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395 [No Abstract] [Full Text] [Related]
22. Direct familial transmission of the Turner phenotype. Nora JJ; Sinha AK Am J Dis Child; 1968 Oct; 116(4):343-50. PubMed ID: 5697967 [No Abstract] [Full Text] [Related]
27. Turner phenotype: mosaic 45,X-47,XY, plus 18. Schinzel A; Schmid W; Prader A J Med Genet; 1974 Mar; 11(1):101-4. PubMed ID: 4135076 [TBL] [Abstract][Full Text] [Related]
28. FAMILIAL MOSAICISM OF A CHROMOSOME 16 ABNORMALITY ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES. TIPS RL; SMITH GS; MEYER DL; PERKINS AL Am J Ment Defic; 1964 Nov; 69():330-40. PubMed ID: 14223550 [No Abstract] [Full Text] [Related]
29. Human chromosome abnormalities as related to physical and mental dysfunction. Heller JH J Hered; 1969; 60(5):239-48. PubMed ID: 4244249 [No Abstract] [Full Text] [Related]
30. 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]
31. A patient with 45,XX,Gminus-46,XX,Gr mosaicism. Blank CE; Lorber J J Med Genet; 1969 Jun; 6(2):220-3. PubMed ID: 5801471 [No Abstract] [Full Text] [Related]
32. The mental implications of sex chromosome aberrations. Forssman H Br J Psychiatry; 1970 Oct; 117(539):353-63. PubMed ID: 4921232 [No Abstract] [Full Text] [Related]
33. [Studying a case of mosaicism XO-XX R]. Burgio GR; Tiepolo L; Biscatti G; Scappaticci S Pediatria (Napoli); 1970; 78(2):113-33. PubMed ID: 5478728 [No Abstract] [Full Text] [Related]
34. [Translocation D-D and Turner's syndrome. Considerations on a rare association of chromosome pathology]. Giovannucci ML; Pierro U; Cordelli F; Paoli A Haematologica; 1969; 54(11):813-26. PubMed ID: 4993250 [No Abstract] [Full Text] [Related]
35. Mental retardation in Turner's syndrome. Nielsen J; Fischer M; Friedrich U J Ment Defic Res; 1973; 17(3):227-30. PubMed ID: 4794978 [No Abstract] [Full Text] [Related]
36. Supernumerary chromosomes in mosaic Turner syndrome. Thong MK; Manonmani V; Norlasiah IS Med J Malaysia; 1996 Dec; 51(4):487-90. PubMed ID: 10968041 [TBL] [Abstract][Full Text] [Related]
37. Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989. Kleczkowska A; Dmoch E; Kubien E; Fryns JP; Van den Berghe H Genet Couns; 1990; 1(3-4):227-33. PubMed ID: 2098046 [TBL] [Abstract][Full Text] [Related]
38. Chromosomal studies in relation to abortion. Adler P; Gierke LW J Am Osteopath Assoc; 1971 Aug; 70(12):1319-23. PubMed ID: 4255173 [No Abstract] [Full Text] [Related]
39. Familial chromosomal aberrations. I. Zellweger H Ann Paediatr; 1966; 206(5):317-32. PubMed ID: 4225154 [No Abstract] [Full Text] [Related]
40. [Mosaicism in ShereshevskiÄ-Turner's syndrome: clinical manifestations and dermatoglyphic characteristics]. Egorkina DA; Gurevich LE; Tomadze AA Sov Med; 1984; (4):43-8. PubMed ID: 6740399 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]