Temple IK - Search Results

1

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

2

Maternal uniparental disomy for chromosome 14.

Temple IK, Cockwell A, Hassold T, Pettay D, Jacobs P. Temple IK, et al. J Med Genet. 1991 Aug;28(8):511-4. doi: 10.1136/jmg.28.8.511. J Med Genet. 1991. PMID: 1681108 Free PMC article.

3

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.

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

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.

6

Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.

Houlston RS, Renshaw RM, James RS, Ironton R, Temple IK. Houlston RS, et al. Among authors: temple ik. J Med Genet. 1994 Nov;31(11):884-7. doi: 10.1136/jmg.31.11.884. J Med Genet. 1994. PMID: 7853376 Free PMC article.

7

Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.

Barber JC, James RS, Patch C, Temple IK. Barber JC, et al. Among authors: temple ik. Am J Med Genet. 1994 Apr 15;50(3):296-9. doi: 10.1002/ajmg.1320500315. Am J Med Genet. 1994. PMID: 8042676

8

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.

9

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

10

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

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