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.
275 related articles for article (PubMed ID: 9238821)
1. [Indications of chromosome and DNA analysis for the diagnosis of genetic diseases]. Romana SP; Gérard B Rev Prat; 1997 Jun; 47(11):1241-52. PubMed ID: 9238821 [No Abstract] [Full Text] [Related]
2. [Determination of chromosome aberrations with the help of DNA arrays]. Rødningen OK; Prescott TE; Hovland R; Eiklid K; Houge G Tidsskr Nor Laegeforen; 2010 May; 130(9):944-7. PubMed ID: 20453958 [No Abstract] [Full Text] [Related]
3. [Use of DNA polymorphism in the diagnosis of human genetic diseases]. Cebrat S Postepy Hig Med Dosw; 1988; 42(5):461-82. PubMed ID: 2908211 [No Abstract] [Full Text] [Related]
4. The emerging genetic theories of unstable DNA, uniparental disomy, and imprinting. Wilkins-Haug L Curr Opin Obstet Gynecol; 1993 Apr; 5(2):179-85. PubMed ID: 8490087 [TBL] [Abstract][Full Text] [Related]
5. The chromosome, its anatomy, and its aberrations. Yang-Feng TL Res Publ Assoc Res Nerv Ment Dis; 1991; 69():19-38. PubMed ID: 2003160 [No Abstract] [Full Text] [Related]
6. [Methods of research on the chromosome level in diagnosing genetic disorders]. Ruffini E Minerva Pediatr; 1989 Sep; 41(9):491-2. PubMed ID: 2586382 [No Abstract] [Full Text] [Related]
7. [Use of the recombination gene technic (gene splicing) in clinical medicine]. Schuler D; Raskó I Orv Hetil; 1985 Feb; 126(8):437-42. PubMed ID: 3885137 [No Abstract] [Full Text] [Related]
9. Spectral karyotyping analysis of head and neck squamous cell carcinoma. Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603 [TBL] [Abstract][Full Text] [Related]
10. "Genetic for medical practitioners". Ambani LM Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087 [No Abstract] [Full Text] [Related]
11. Strategies and logistical requirements for efficient testing in genetic disease. Jackson-Cook C; Pandya A Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226 [TBL] [Abstract][Full Text] [Related]
12. Primed IN situ labelling (PRINS) as a rational procedure for identification of marker chromosomes using a panel of primers differentially tagging the human chromosomes. Hindkjaer J; Brandt CA; Strømkjaer H; Koch J; Kølvraa S; Bolund L Clin Genet; 1996 Dec; 50(6):437-41. PubMed ID: 9147869 [TBL] [Abstract][Full Text] [Related]