Temple IK - Search Results

1

Quality of life after repair of tetralogy of Fallot.

Walker WT, Temple IK, Gnanapragasam JP, Goddard JR, Brown EM. Walker WT, et al. Among authors: temple ik. Cardiol Young. 2002 Dec;12(6):549-53. doi: 10.1017/s1047951102000999. Cardiol Young. 2002. PMID: 12636003

2

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.

Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR. Webber SA, et al. Among authors: temple ik. J Pediatr. 1996 Jul;129(1):26-32. doi: 10.1016/s0022-3476(96)70186-5. J Pediatr. 1996. PMID: 8757559

3

Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports.

Law CJ, Fisher AM, Temple IK. Law CJ, et al. Among authors: temple ik. J Med Genet. 1998 Aug;35(8):685-9. doi: 10.1136/jmg.35.8.685. J Med Genet. 1998. PMID: 9719381 Free PMC article. Review.

4

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

5

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

6

Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.

Gardner RJ, Mungall AJ, Dunham I, Barber JC, Shield JP, Temple IK, Robinson DO. Gardner RJ, et al. Among authors: temple ik. J Med Genet. 1999 Mar;36(3):192-6. J Med Genet. 1999. PMID: 10204843 Free PMC article.

7

A female case of Sedaghatian type spondylometaphyseal dysplasia.

Foulds N, Fairhurst J, Temple IK, Cade S, Groves C, Lancaster T. Foulds N, et al. Among authors: temple ik. Am J Med Genet A. 2003 May 1;118A(4):377-81. doi: 10.1002/ajmg.a.10199. Am J Med Genet A. 2003. PMID: 12687672

8

Kabuki syndrome: new ocular findings but no evidence of 8p22-p23.1 duplications in a clinically defined cohort.

Turner C, Lachlan K, Amerasinghe N, Hodgkins P, Maloney V, Barber J, Temple IK. Turner C, et al. Among authors: temple ik. Eur J Hum Genet. 2005 Jun;13(6):716-20. doi: 10.1038/sj.ejhg.5201377. Eur J Hum Genet. 2005. PMID: 15785777

9

6q24 transient neonatal diabetes.

Temple IK, Shield JP. Temple IK, et al. Rev Endocr Metab Disord. 2010 Sep;11(3):199-204. doi: 10.1007/s11154-010-9150-4. Rev Endocr Metab Disord. 2010. PMID: 20922569 Review.

10

Diaphragmatic herniae and translocations involving 8q22 in two patients.

Temple IK, Barber JC, James RS, Burge D. Temple IK, et al. J Med Genet. 1994 Sep;31(9):735-7. doi: 10.1136/jmg.31.9.735. J Med Genet. 1994. PMID: 7815446 Free PMC article.

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