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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
262 related items for PubMed ID: 12875676
1. Prenatal diagnosis of Werdnig-Hoffmann disease in China. Feng J, Toshiyuki Y. Chin Med J (Engl); 2003 May; 116(5):673-5. PubMed ID: 12875676 [Abstract] [Full Text] [Related]
2. Prenatal prediction of spinal muscular atrophy by SMN deletion analysis. Dhamcharee V, Mutirangura A, Tannirandom Y, Jongpiputvanich S, Romyanan O. Southeast Asian J Trop Med Public Health; 1999 May; 30 Suppl 2():186-7. PubMed ID: 11400766 [Abstract] [Full Text] [Related]
3. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells. Wu T, Ding XS, Li WL, Yao J, Deng XX. Chin Med J (Engl); 2005 Aug 05; 118(15):1274-7. PubMed ID: 16117881 [Abstract] [Full Text] [Related]
4. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes. Stipoljev F, Sertić J, Latin V, Rukavina-Stavljenić A, Kurjak A. Croat Med J; 1999 Sep 05; 40(3):433-7. PubMed ID: 10411975 [Abstract] [Full Text] [Related]
5. [Gene diagnosis for spinal muscular atrophy and its application study]. Cao DH, Ren MH, Lin CK, Cui WT, Ma HW, Wu YY, Jin CL. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 05; 26(3):306-9. PubMed ID: 19504445 [Abstract] [Full Text] [Related]
6. Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families. Savas S, Eraslan S, Kantarci S, Karaman B, Acarsoz D, Tükel T, Cogulu O, Ozkinay F, Basaran S, Aydinli K, Yuksel-Apak M, Kirdar B. Prenat Diagn; 2002 Aug 05; 22(8):703-9. PubMed ID: 12210580 [Abstract] [Full Text] [Related]
9. Prenatal diagnosis for risk of spinal muscular atrophy. Cuscó I, Barceló MJ, Soler C, Parra J, Baiget M, Tizzano E. BJOG; 2002 Nov 05; 109(11):1244-9. PubMed ID: 12452462 [Abstract] [Full Text] [Related]
10. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis. Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N. Arch Neurol; 2007 Feb 05; 64(2):225-31. PubMed ID: 17296838 [Abstract] [Full Text] [Related]
11. Preserved umbilical cord facilitates antenatal diagnosis of spinal muscular atrophy. Kabra M, Arora S, Maria A, Aggarwal R. Indian Pediatr; 2003 May 05; 40(5):415-8. PubMed ID: 12768044 [Abstract] [Full Text] [Related]
12. [Werdnig-Hoffmann disease. The first prenatal diagnosis in Cuba]. Acevedo-López AM, Zaldívar-Vaillant T, Hernández-Chico C, Moreno F, Rosich-Capablanca G, Guerra-Badía R. Rev Neurol; 2003 May 05; 29(12):1172-5. PubMed ID: 10652743 [Abstract] [Full Text] [Related]
16. [Survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletion in patients with spinal muscular atrophy]. Ma S, Yuan L, Liu T, Yang T, Zhou W, Wu H. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Dec 01; 22(6):551-4. PubMed ID: 12903402 [Abstract] [Full Text] [Related]
17. Genetic diagnosis of Werdnig-Hoffmann disease: a problem for application to prenatal diagnosis. Migita M, Migita M, Uchikoba Y, Orimo H, Shimada T, Shimada T, Matsumoto T, Hayakawa J, Fujino O, Saitoh M, Fukunaga Y. J Nippon Med Sch; 2003 Feb 01; 70(1):45-8. PubMed ID: 12646976 [Abstract] [Full Text] [Related]
18. [An analysis of chimeric SMN genes--new possibilities in the study of the molecular genetic nature of mutations and in the diagnosis of spinal muscular atrophy (SMA)]. Ekshiian AIu, Livshits LA. Tsitol Genet; 1999 Feb 01; 33(3):21-6. PubMed ID: 10474859 [Abstract] [Full Text] [Related]
19. [A molecular genetic analysis of spinal muscular atrophy (SMA) in families at high risk from different regions of Ukraine]. Ekshiian AIu, Livshits LA, Bychkova AM, Afanas'eva NA, Bariliak IR. Tsitol Genet; 1997 Feb 01; 31(6):75-81. PubMed ID: 9591348 [Abstract] [Full Text] [Related]
20. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests. Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G. Neurology; 2005 Nov 22; 65(10):1631-5. PubMed ID: 16301493 [Abstract] [Full Text] [Related] Page: [Next] [New Search]