ExLibris header image
SFX Logo
Title: Regional localization of the gene for human phosphoribosylpyrophosphate synthetase on the X chromosome
Source:

Science [0036-8075] Becker, M A yr:1979


Collapse list of basic services Basic
Sorry, no full text available...
Please use the document delivery service (see below)  
Holding information
Holdings in library search engine ALBERT GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. McCarthy, Gillian T. "A population study of Lesch-Nyhan disease in the UK." Developmental medicine and child neurology 53.1 (2011): 34-39. Link to Full Text for this item Link to SFX for this item
2. Doucet, Brian P. "Late diagnosis of Lesch-Nyhan disease variant." BMJ Case Reports 2013.dec10 1 (2013). Link to Full Text for this item Link to SFX for this item
3. Dauphinot, L. "Transcriptomic Approach to Lesch-Nyhan Disease." Nucleosides, nucleotides & nucleic acids 33.4-6 (2014): 208-217. Link to SFX for this item
4. Nguyen, Khue V. "Lesch–Nyhan Variant Syndrome: Real-Time RT-PCR for mRNA Quantification in Variable Presentation in Three Affected Family Members." Nucleosides, nucleotides & nucleic acids 31.8 (2012): 616-629. Link to SFX for this item
5. Schretlen, David J J. "Behavioral aspects of Lesch-Nyhan disease and its variants." Developmental medicine and child neurology 47.10: 673-677. Link to SFX for this item
6. Eddey, Gary E L. "Modes and patterns of self-mutilation in persons with Lesch-Nyhan disease." Developmental medicine and child neurology 45.3 (2003): 167-171. Link to Full Text for this item Link to SFX for this item
7. "FIRST-TRIMESTER DIAGNOSIS OF LESCH-NYHAN SYNDROME." The lancet. 324.8413: 1180-1183. Link to SFX for this item
8. Ceballos Picot, I. "New biomarkers for early diagnosis of Lesch-Nyhan disease revealed by metabolic analysis on a large cohort of patients." Orphanet journal of rare diseases 10.1 (2015): 7-7. Link to Full Text for this item Link to SFX for this item
9. "Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome." Nucleosides, nucleotides & nucleic acids 35.8 (2016): 426-434. Link to SFX for this item
10. Fu, R. "Genotypic and phenotypic spectrum in attenuated variants of Lesch-Nyhan disease." Molecular genetics and metabolism 112.4 (2014): 280-285. Link to SFX for this item
11. Cauwels, R. "Self-mutilation behaviour in Lesch-Nyhan syndrome." Journal of oral pathology & medicine 34.9 (2005): 573-5. Link to Full Text for this item Link to SFX for this item
12. MacDonald, Jennifer E. "Brief functional analysis and treatment of eye poking." Behavioral interventions 17.4 (2002): 261-270. Link to Full Text for this item Link to SFX for this item
13. Olson, L. "A review of behavioral treatments used for Lesch-Nyhan syndrome." Behavior modification 24.2 (2000): 202-22. Link to Full Text for this item Link to SFX for this item
14. Shu, L. "Long-term glue-sniffing: Report of six cases." The International journal of psychiatry in medicine 33.2 (2003): 163-168. Link to SFX for this item
15. McCarthy, G. "Medical diagnosis, management and treatment of Lesch Nyhan disease." Nucleosides, nucleotides & nucleic acids 23.8 (2004): 1147-52. Link to SFX for this item
16. Chandekar, P. "Lesch-nyhan syndrome in an Indian child." Indian journal of dermatology. 60.3: 298-300. Link to SFX for this item
17. Liu, N. "Prenatal diagnosis based onHPRT1gene mutation in a Lesch–Nyhan family." Journal of Obstetrics and Gynaecology 35.5 (2015): 490-493. Link to SFX for this item
18. "Studies in the area of biochemistry reported from University of Minnesota, Department of Pediatrics." Science Letter (2010): 5231-. Link to SFX for this item
19. Nguyen, Khue V. "Epigenetic regulation in amyloid precursor protein and the Lesch-Nyhan syndrome." Biochemical and biophysical research communications 446.4 (2014): 1091-1095. Link to SFX for this item
20. Russo, D. "High frequency of genomic deletions induced by Me-lex, a sequence selective N3-adenine methylating agent, at the Hprt locus in Chinese hamster ovary cells." Mutation research 671.1 (2009): 58-66. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.