Temple IK - Search Results

1

An imprinted locus associated with transient neonatal diabetes mellitus.

Gardner RJ, Mackay DJ, Mungall AJ, Polychronakos C, Siebert R, Shield JP, Temple IK, Robinson DO. Gardner RJ, et al. Among authors: temple ik. Hum Mol Genet. 2000 Mar 1;9(4):589-96. doi: 10.1093/hmg/9.4.589. Hum Mol Genet. 2000. PMID: 10699182

2

An imprinted gene(s) for diabetes?

Temple IK, James RS, Crolla JA, Sitch FL, Jacobs PA, Howell WM, Betts P, Baum JD, Shield JP. Temple IK, et al. Nat Genet. 1995 Feb;9(2):110-2. doi: 10.1038/ng0295-110. Nat Genet. 1995. PMID: 7719335 No abstract available.

3

A search for uniparental disomy in carriers of supernumerary marker chromosomes.

James RS, Temple IK, Dennis NR, Crolla JA. James RS, et al. Among authors: temple ik. Eur J Hum Genet. 1995;3(1):21-6. doi: 10.1159/000472270. Eur J Hum Genet. 1995. PMID: 7767653

4

A systematic search for uniparental disomy in carriers of chromosome translocations.

James RS, Temple IK, Patch C, Thompson EM, Hassold T, Jacobs PA. James RS, et al. Among authors: temple ik. Eur J Hum Genet. 1994;2(2):83-95. doi: 10.1159/000472348. Eur J Hum Genet. 1994. PMID: 8044660 Review.

5

A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.

Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK. Wilkinson TA, et al. Among authors: temple ik. Prenat Diagn. 1996 Apr;16(4):371-4. doi: 10.1002/(SICI)1097-0223(199604)16:4<371::AID-PD866>3.0.CO;2-S. Prenat Diagn. 1996. PMID: 8734817

6

Unbalanced translocation in a mother and her son in one of two 5;10 translocation families.

Barber JC, Temple IK, Campbell PL, Collinson MN, Campbell CM, Renshaw RM, Dennis NR. Barber JC, et al. Among authors: temple ik. Am J Med Genet. 1996 Mar 1;62(1):84-90. doi: 10.1002/(SICI)1096-8628(19960301)62:1<84::AID-AJMG17>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8779332

7

Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23.

Temple IK, Gardner RJ, Robinson DO, Kibirige MS, Ferguson AW, Baum JD, Barber JC, James RS, Shield JP. Temple IK, et al. Hum Mol Genet. 1996 Aug;5(8):1117-21. doi: 10.1093/hmg/5.8.1117. Hum Mol Genet. 1996. PMID: 8842729

8

Aetiopathology and genetic basis of neonatal diabetes.

Shield JP, Gardner RJ, Wadsworth EJ, Whiteford ML, James RS, Robinson DO, Baum JD, Temple IK. Shield JP, et al. Among authors: temple ik. Arch Dis Child Fetal Neonatal Ed. 1997 Jan;76(1):F39-42. doi: 10.1136/fn.76.1.f39. Arch Dis Child Fetal Neonatal Ed. 1997. PMID: 9059185 Free PMC article.

9

A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis.

Robinson DO, Bunyan DJ, Gabb HA, Temple IK, Yau SC. Robinson DO, et al. Among authors: temple ik. Hum Genet. 1997 May;99(5):658-62. doi: 10.1007/s004390050424. Hum Genet. 1997. PMID: 9150736

10

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: temple ik. J Med Genet. 1997 May;34(5):353-9. doi: 10.1136/jmg.34.5.353. J Med Genet. 1997. PMID: 9152830 Free PMC article.

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