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.
176 related articles for article (PubMed ID: 4929739)
21. [Molecular genetics of red-green color blindness]. Ladekjaer-Mikkelsen AS; Jensen H; Rosenberg T; Jørgensen AL Ugeskr Laeger; 1995 Aug; 157(35):4808-12. PubMed ID: 7676516 [TBL] [Abstract][Full Text] [Related]
22. Sex chromosomal aberration syndromes. Jackson JF Ala J Med Sci; 1974 Oct; 11(4):302-7. PubMed ID: 4460716 [No Abstract] [Full Text] [Related]
23. Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients. Soltan HC J Med Genet; 1968 Sep; 5(3):173-80. PubMed ID: 5304308 [No Abstract] [Full Text] [Related]
24. Analysis of the SRY gene in a girl with 45,X/46,XY genotype. Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431 [TBL] [Abstract][Full Text] [Related]
25. [Systematic study of Barr bodies in 2500 infants with severe congenital heart defects]. Gautier M; Hugon RN Ann Genet; 1973 Mar; 16(1):67-8. PubMed ID: 4541813 [No Abstract] [Full Text] [Related]
26. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes. Zaki MS; Kamel AA; El-Ruby M Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882 [TBL] [Abstract][Full Text] [Related]
27. Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients. Fryns JP; Kleczkowska A; Kubień E; Van den Berghe H Acta Paediatr Scand Suppl; 1984; 313():1-23. PubMed ID: 6241420 [TBL] [Abstract][Full Text] [Related]
28. Genetics and physiology of color vision V. Waaler GH J Oslo City Hosp; 1978 Sep; 28(9):125-8. PubMed ID: 308531 [No Abstract] [Full Text] [Related]
31. A heterotic model for the evolution of duplications. Spofford JB Brookhaven Symp Biol; 1972; 23():121-43. PubMed ID: 5047197 [No Abstract] [Full Text] [Related]
32. [On a case of XO gonado-somatic dysgenesis]. Curcio S Arch Ostet Ginecol; 1967; 72(5):540-6. PubMed ID: 5305366 [No Abstract] [Full Text] [Related]
33. [Two cases of Klinefelter's syndrome with mosaicism (46,XY-47,XXY), one of which is associated with protanopia and the other with unilateral corneal opacities]. Boreux G; Tajmirova O; Klein D; Gauthier G; Felgenhauer WR Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1969; 44(3-4):suppl 55-64. PubMed ID: 5315152 [No Abstract] [Full Text] [Related]
34. Association between the degree of mosaicism and the severity of syndrome in Turner mosaics and Klinefelter mosaics. Sarkar R; Marimuthu KM Clin Genet; 1983 Dec; 24(6):420-8. PubMed ID: 6652955 [TBL] [Abstract][Full Text] [Related]
35. Abnormal gonadal differentiation in XY females and XX males. Ferguson-Smith MA Birth Defects Orig Artic Ser; 1971 May; 7(6):204-9. PubMed ID: 5173163 [TBL] [Abstract][Full Text] [Related]
36. Color vision in patients with the Hermansky-Pudlak syndrome. Rodríguez JA; Blasini M; Blasini M; Townsend W; Izquierdo NJ Bol Asoc Med P R; 2004; 96(2):84-90. PubMed ID: 15580910 [TBL] [Abstract][Full Text] [Related]
39. [Genetics of congenital color vision defects. I. Common types of color blindness]. Krawczyński MR Klin Oczna; 1995; 97(1-2):34-8. PubMed ID: 7637311 [TBL] [Abstract][Full Text] [Related]
40. Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52. Panarello C; Acquila M; Caprino D; Gimelli G; Pecorara M; Mori PG Cytogenet Cell Genet; 1992; 59(4):241-2. PubMed ID: 1544315 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]