Coffey R - Search Results

1

Risk estimation and screening in families of patients with medullary thyroid carcinoma.

Ponder BA, Ponder MA, Coffey R, Pembrey ME, Gagel RF, Telenius-Berg M, Semple P, Easton DF. Ponder BA, et al. Among authors: coffey r. Lancet. 1988 Feb 20;1(8582):397-401. doi: 10.1016/s0140-6736(88)91191-9. Lancet. 1988. PMID: 2893198

2

Family screening in medullary thyroid carcinoma presenting without a family history.

Ponder BA, Finer N, Coffey R, Harmer CL, Maisey M, Ormerod MG, Pembrey ME, Ponder MA, Rosswick P, Shalet S. Ponder BA, et al. Among authors: coffey r. Q J Med. 1988 Apr;67(252):299-308. Q J Med. 1988. PMID: 2905066

3

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.

Burn J, Brennan P, Little J, Holloway S, Coffey R, Somerville J, Dennis NR, Allan L, Arnold R, Deanfield JE, Godman M, Houston A, Keeton B, Oakley C, Scott O, Silove E, Wilkinson J, Pembrey M, Hunter AS. Burn J, et al. Among authors: coffey r. Lancet. 1998 Jan 31;351(9099):311-6. doi: 10.1016/s0140-6736(97)06486-6. Lancet. 1998. PMID: 9652610

4

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.

Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R. Gausden E, et al. Among authors: coffey r. Clin Endocrinol (Oxf). 1996 Apr;44(4):441-6. doi: 10.1046/j.1365-2265.1996.714536.x. Clin Endocrinol (Oxf). 1996. PMID: 8706311

5

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage.

Gausden E, Coyle B, Armour JA, Coffey R, Grossman A, Fraser GR, Winter RM, Pembrey ME, Kendall-Taylor P, Stephens D, Luxon LM, Phelps PD, Reardon W, Trembath R. Gausden E, et al. Among authors: coffey r. J Med Genet. 1997 Feb;34(2):126-9. doi: 10.1136/jmg.34.2.126. J Med Genet. 1997. PMID: 9039988 Free PMC article.

6

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.

Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W, Trembath R. Coyle B, et al. Among authors: coffey r. Nat Genet. 1996 Apr;12(4):421-3. doi: 10.1038/ng0496-421. Nat Genet. 1996. PMID: 8630497

7

Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region.

Chung E, Coffey R, Parker K, Tam P, Pembrey ME, Gardiner RM. Chung E, et al. Among authors: coffey r. J Med Genet. 1993 May;30(5):393-5. doi: 10.1136/jmg.30.5.393. J Med Genet. 1993. PMID: 8320701 Free PMC article.

8

Abnormal audiograms and elevated acoustic reflex thresholds in obligate carriers of autosomal recessive non-syndromic hearing loss.

Cohen M, Francis M, Coffey R, Pembrey ME, Luxon LM. Cohen M, et al. Among authors: coffey r. Acta Otolaryngol. 1997 May;117(3):337-42. doi: 10.3109/00016489709113404. Acta Otolaryngol. 1997. PMID: 9199518

9

Dips on Békésy or audioscan fail to identify carriers of autosomal recessive non-syndromic hearing loss.

Cohen M, Francis M, Luxon LM, Bellman S, Coffey R, Pembrey M. Cohen M, et al. Among authors: coffey r. Acta Otolaryngol. 1996 Jul;116(4):521-7. doi: 10.3109/00016489609137883. Acta Otolaryngol. 1996. PMID: 8831836

10

Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosis.

Lambert SR, Kriss A, Taylor D, Coffey R, Pembrey M. Lambert SR, et al. Among authors: coffey r. Am J Ophthalmol. 1989 Jun 15;107(6):624-31. doi: 10.1016/0002-9394(89)90259-6. Am J Ophthalmol. 1989. PMID: 2658617 Review.

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