Prior TW - Search Results

1

Case report on hereditary non-polyposis colon cancer (HNPCC) in Nigeria.

Adebamowo CA, Adeyi O, Pyatt R, Prior TW, Chadwick RB, de la Chapelle A. Adebamowo CA, et al. Among authors: prior tw. Afr J Med Med Sci. 2000 Mar;29(1):71-3. Afr J Med Med Sci. 2000. PMID: 11379475

2

The I1307K polymorphism of the APC gene in colorectal cancer.

Prior TW, Chadwick RB, Papp AC, Arcot AN, Isa AM, Pearl DK, Stemmermann G, Percesepe A, Loukola A, Aaltonen LA, De La Chapelle A. Prior TW, et al. Gastroenterology. 1999 Jan;116(1):58-63. doi: 10.1016/s0016-5085(99)70229-5. Gastroenterology. 1999. PMID: 9869603 Clinical Trial.

3

Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testing.

Pyatt R, Chadwick RB, Johnson CK, Adebamowo C, de la Chapelle A, Prior TW. Pyatt R, et al. Among authors: prior tw. Am J Pathol. 1999 Aug;155(2):349-53. doi: 10.1016/S0002-9440(10)65131-0. Am J Pathol. 1999. PMID: 10433928 Free PMC article.

4

Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.

Chadwick RB, Pyatt RE, Niemann TH, Richards SK, Johnson CK, Stevens MW, Meek JE, Hampel H, Prior TW, de la Chapelle A. Chadwick RB, et al. Among authors: prior tw. J Med Genet. 2001 Jul;38(7):461-6. doi: 10.1136/jmg.38.7.461. J Med Genet. 2001. PMID: 11474654 Free PMC article. No abstract available.

5

A feasibility study for the newborn screening of spinal muscular atrophy.

Pyatt RE, Prior TW. Pyatt RE, et al. Among authors: prior tw. Genet Med. 2006 Jul;8(7):428-37. doi: 10.1097/01.gim.0000227970.60450.b2. Genet Med. 2006. PMID: 16845275 Free article.

6

Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.

Pyatt RE, Nakagawa H, Hampel H, Sedra M, Fuchik MB, Comeras I, de la Chapelle A, Prior TW. Pyatt RE, et al. Among authors: prior tw. Clin Genet. 2003 Mar;63(3):215-8. doi: 10.1034/j.1399-0004.2003.00040.x. Clin Genet. 2003. PMID: 12694232

7

Mutation screening in juvenile polyposis syndrome.

Pyatt RE, Pilarski R, Prior TW. Pyatt RE, et al. Among authors: prior tw. J Mol Diagn. 2006 Feb;8(1):84-8. doi: 10.2353/jmoldx.2006.050072. J Mol Diagn. 2006. PMID: 16436638 Free PMC article.

8

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Hampel H, et al. Among authors: prior tw. N Engl J Med. 2005 May 5;352(18):1851-60. doi: 10.1056/NEJMoa043146. N Engl J Med. 2005. PMID: 15872200 Free article.

9

Polymorphisms in a pseudogene highly homologous to PMS2.

Chadwick RB, Meek JE, Prior TW, Peltomaki P, de La Chapelle A. Chadwick RB, et al. Among authors: prior tw. Hum Mutat. 2000 Dec;16(6):530. doi: 10.1002/1098-1004(200012)16:6<530::AID-HUMU15>3.0.CO;2-6. Hum Mutat. 2000. PMID: 11102987

10

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome.

Mailman MD, Hemingway T, Darsey RL, Glasure CE, Huang Y, Chadwick RB, Heinz JW, Papp AC, Snyder PJ, Sedra MS, Schafer RW, Abuelo DN, Reich EW, Theil KS, Burghes AH, de la Chapelle A, Prior TW. Mailman MD, et al. Among authors: prior tw. Hum Genet. 2001 Feb;108(2):109-15. doi: 10.1007/s004390000446. Hum Genet. 2001. PMID: 11281448

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