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.
115 related articles for article (PubMed ID: 20642358)
21. Gene identification by chromosomal in-situ hybridization, microdissection and polymerase chain reaction amplification. Sallie R Med Hypotheses; 1996 Jun; 46(6):533-5. PubMed ID: 8803937 [TBL] [Abstract][Full Text] [Related]
22. Identifying genes within the genome: new ways for finding the needle in a haystack. Hochgeschwender U; Brennan MB Bioessays; 1991 Mar; 13(3):139-44. PubMed ID: 1872824 [No Abstract] [Full Text] [Related]
23. The Wilhelmine E. Key 1979 Invitational Lecture: The anatomy of the human genome. McKusick VA J Hered; 1980; 71(6):370-91. PubMed ID: 6783695 [No Abstract] [Full Text] [Related]
24. [Segment duplications in the human genome]. Lakrua ME; Oparina NIu; Mashkova TD Mol Biol (Mosk); 2003; 37(2):212-20. PubMed ID: 12723468 [TBL] [Abstract][Full Text] [Related]
25. Laboratory investigations in genetic syndromes: examples of clinical approach in the neonatal unit. De Sanctis L; Giuffrè M Minerva Pediatr; 2010 Jun; 62(3 Suppl 1):193-5. PubMed ID: 21089740 [TBL] [Abstract][Full Text] [Related]
26. Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human genomic disorders. Sankaranarayanan K; Wassom JS Mutat Res; 2005 Oct; 578(1-2):333-70. PubMed ID: 16084534 [TBL] [Abstract][Full Text] [Related]
27. DNA clustering and genome complexity. Dios F; Barturen G; Lebrón R; Rueda A; Hackenberg M; Oliver JL Comput Biol Chem; 2014 Dec; 53 Pt A():71-8. PubMed ID: 25182383 [TBL] [Abstract][Full Text] [Related]
28. Deletions of chromosomal regulatory boundaries are associated with congenital disease. Ibn-Salem J; Köhler S; Love MI; Chung HR; Huang N; Hurles ME; Haendel M; Washington NL; Smedley D; Mungall CJ; Lewis SE; Ott CE; Bauer S; Schofield PN; Mundlos S; Spielmann M; Robinson PN Genome Biol; 2014 Sep; 15(9):423. PubMed ID: 25315429 [TBL] [Abstract][Full Text] [Related]
29. Identification of human haploinsufficient genes and their genomic proximity to segmental duplications. Dang VT; Kassahn KS; Marcos AE; Ragan MA Eur J Hum Genet; 2008 Nov; 16(11):1350-7. PubMed ID: 18523451 [TBL] [Abstract][Full Text] [Related]
30. Disease genes and chromosomes: disease maps of the human genome. Chromosome 15. Gilbert F Genet Test; 1999; 3(3):309-22. PubMed ID: 10495933 [No Abstract] [Full Text] [Related]
31. Epialleles and common disease. Peedicayil J Med Hypotheses; 2005; 64(1):215. PubMed ID: 15533644 [No Abstract] [Full Text] [Related]