Cox TM - Search Results

1

Aldolase B mutations in Italian families affected by hereditary fructose intolerance.

Sebastio G, de Franchis R, Strisciuglio P, Andria G, Dionisi Vici C, Sabetta G, Gatti R, Cross NC, Cox TM. Sebastio G, et al. Among authors: cox tm. J Med Genet. 1991 Apr;28(4):241-3. doi: 10.1136/jmg.28.4.241. J Med Genet. 1991. PMID: 1856829 Free PMC article.

2

Null alleles of the aldolase B gene in patients with hereditary fructose intolerance.

Ali M, Tunçman G, Cross NC, Vidailhet M, Bökesoy I, Gitzelmann R, Cox TM. Ali M, et al. Among authors: cox tm. J Med Genet. 1994 Jun;31(6):499-503. doi: 10.1136/jmg.31.6.499. J Med Genet. 1994. PMID: 8071980 Free PMC article.

3

Partial aldolase B gene deletions in hereditary fructose intolerance.

Cross NC, Cox TM. Cross NC, et al. Among authors: cox tm. Am J Hum Genet. 1990 Jul;47(1):101-6. Am J Hum Genet. 1990. PMID: 2349937 Free PMC article.

4

Molecular analysis of aldolase B genes in the diagnosis of hereditary fructose intolerance in the United Kingdom.

Cross NC, Cox TM. Cross NC, et al. Among authors: cox tm. Q J Med. 1989 Nov;73(271):1015-20. Q J Med. 1989. PMID: 2623136

5

Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.

Ali M, Sebastio G, Cox TM. Ali M, et al. Among authors: cox tm. Hum Mol Genet. 1994 Apr;3(4):684. Hum Mol Genet. 1994. PMID: 8069328 No abstract available.

6

Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.

Ali M, Sebastio G, Cox TM. Ali M, et al. Among authors: cox tm. Hum Mol Genet. 1994 Jan;3(1):203-4. doi: 10.1093/hmg/3.1.203. Hum Mol Genet. 1994. PMID: 8162030 No abstract available.

7

Hereditary fructose intolerance.

Cross NC, Cox TM. Cross NC, et al. Among authors: cox tm. Int J Biochem. 1990;22(7):685-9. doi: 10.1016/0020-711x(90)90002-k. Int J Biochem. 1990. PMID: 2205519 Review. No abstract available.

8

A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia.

Cross NC, Stojanov LM, Cox TM. Cross NC, et al. Among authors: cox tm. Nucleic Acids Res. 1990 Apr 11;18(7):1925. doi: 10.1093/nar/18.7.1925. Nucleic Acids Res. 1990. PMID: 2336380 Free PMC article.

9

Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.

Cross NC, Tolan DR, Cox TM. Cross NC, et al. Among authors: cox tm. Cell. 1988 Jun 17;53(6):881-5. doi: 10.1016/s0092-8674(88)90349-2. Cell. 1988. PMID: 3383242

10

Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population.

James CL, Rellos P, Ali M, Heeley AF, Cox TM. James CL, et al. Among authors: cox tm. J Med Genet. 1996 Oct;33(10):837-41. doi: 10.1136/jmg.33.10.837. J Med Genet. 1996. PMID: 8933337 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

276 results

Search Page

Filters