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.
138 related articles for article (PubMed ID: 7372336)
21. Prophase analysis of ring chromosome 13--an attempt at phenotype-karyotype correlation. Lagergren M; Börjeson M; Mitelman F Hereditas; 1980; 93(2):231-3. PubMed ID: 7440241 [No Abstract] [Full Text] [Related]
23. Supernumerary chromosomes in six patients. Yip MY; Mark J; Hultén M Clin Genet; 1982 Jun; 21(6):397-406. PubMed ID: 6957276 [No Abstract] [Full Text] [Related]
24. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22). Ohdo S; Madokoro H; Hayakawa K J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050 [No Abstract] [Full Text] [Related]
25. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome. Watt JL; Olson IA; Johnston AW; Ross HS; Couzin DA; Stephen GS J Med Genet; 1985 Aug; 22(4):283-7. PubMed ID: 4045954 [TBL] [Abstract][Full Text] [Related]
26. A case of 21q--syndrome with normal SOD-1 activity. Yamamoto Y; Ogasawara N; Gotoh A; Komiya H; Nakai H; Kuroki Y Hum Genet; 1979 May; 48(3):321-7. PubMed ID: 468232 [TBL] [Abstract][Full Text] [Related]
27. Three cases of 16q duplication. Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771 [No Abstract] [Full Text] [Related]
29. Two cases of ring chromosome 11. Romain DR; Gebbie OB; Parfitt RG; Columbano-Green LM; Smythe RH; Chapman CJ; Kerr A J Med Genet; 1983 Oct; 20(5):380-2. PubMed ID: 6315941 [TBL] [Abstract][Full Text] [Related]
30. Indications for chromosome analysis illustrated by a case of ring 22. Howard-Peebles PN J Hered; 1977; 68(4):268-9. PubMed ID: 411817 [TBL] [Abstract][Full Text] [Related]
31. Variability of r(22) chromosomes phenotypical expression. Dallapiccola B; Brinchi V; Curatolo P Acta Genet Med Gemellol (Roma); 1977; 26(3-4):287-90. PubMed ID: 613695 [No Abstract] [Full Text] [Related]
32. [Value of silver staining technics for the study of acrocentric ring chromosomes and supernumerary microchromosomes]. Teyssier M; Moreau N C R Seances Soc Biol Fil; 1984; 178(3):251-6. PubMed ID: 6208982 [TBL] [Abstract][Full Text] [Related]
33. An apparent de novo terminal deletion of chromosome 2 (pter----p24:). Francis GL; Flannery DB; Byrd JR; Fisher ST J Med Genet; 1990 Feb; 27(2):137-8. PubMed ID: 2319584 [No Abstract] [Full Text] [Related]
34. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S Cytogenet Genome Res; 2005; 111(2):171-4. PubMed ID: 16103660 [TBL] [Abstract][Full Text] [Related]
35. A case of D13 ring chromosome. Cossu P; Diana G; Mameli M; Cardia S; Milia A; Floris G; Cao A Hum Genet; 1979 Jan; 46(1):111-4. PubMed ID: 429001 [TBL] [Abstract][Full Text] [Related]
37. Interstitial deletion of chromosome 13: prognosis and adult phenotype. Dean JC; Simpson S; Couzin DA; Stephen GS J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369 [TBL] [Abstract][Full Text] [Related]
38. Chromosome 20 long arm deletion in an elderly malformed man. Shabtai F; Ben-Sasson E; Arieli S; Grinblat J J Med Genet; 1993 Feb; 30(2):171-3. PubMed ID: 8445626 [TBL] [Abstract][Full Text] [Related]
39. [Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome]. Han X; Zhang JM; Jiang WT; Hu Q; Tao J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):361-6. PubMed ID: 20677137 [TBL] [Abstract][Full Text] [Related]
40. Complex structural rearrangement of chromosomes 7, 10, 14 and 21. de Asis ML; Saito F; Tonomura A Jinrui Idengaku Zasshi; 1984 Dec; 29(4):453-9. PubMed ID: 6535858 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]