Coffey R - Search Results

1

Alström syndrome. Report of 22 cases and literature review.

Russell-Eggitt IM, Clayton PT, Coffey R, Kriss A, Taylor DS, Taylor JF. Russell-Eggitt IM, et al. Among authors: coffey r. Ophthalmology. 1998 Jul;105(7):1274-80. doi: 10.1016/S0161-6420(98)97033-6. Ophthalmology. 1998. PMID: 9663233 Review.

2

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.

3

Concordance and recessive inheritance of Leber congenital amaurosis.

Lambert SR, Sherman S, Taylor D, Kriss A, Coffey R, Pembrey M. Lambert SR, et al. Among authors: coffey r. Am J Med Genet. 1993 May 15;46(3):275-7. doi: 10.1002/ajmg.1320460307. Am J Med Genet. 1993. PMID: 8488871

4

Pendred syndrome--100 years of underascertainment?

Reardon W, Coffey R, Phelps PD, Luxon LM, Stephens D, Kendall-Taylor P, Britton KE, Grossman A, Trembath R. Reardon W, et al. Among authors: coffey r. QJM. 1997 Jul;90(7):443-7. doi: 10.1093/qjmed/90.7.443. QJM. 1997. PMID: 9302427

5

Radiological malformations of the ear in Pendred syndrome.

Phelps PD, Coffey RA, Trembath RC, Luxon LM, Grossman AB, Britton KE, Kendall-Taylor P, Graham JM, Cadge BC, Stephens SG, Pembrey ME, Reardon W. Phelps PD, et al. Among authors: coffey ra. Clin Radiol. 1998 Apr;53(4):268-73. doi: 10.1016/s0009-9260(98)80125-6. Clin Radiol. 1998. PMID: 9585042

6

Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.

Reardon W, Coffey R, Chowdhury T, Grossman A, Jan H, Britton K, Kendall-Taylor P, Trembath R. Reardon W, et al. Among authors: coffey r. J Med Genet. 1999 Aug;36(8):595-8. J Med Genet. 1999. PMID: 10465108 Free PMC article.

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

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

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