Bellman SC - Search Results

1

Phenotypic manifestations of branchio-oto-renal syndrome.

Chen A, Francis M, Ni L, Cremers CW, Kimberling WJ, Sato Y, Phelps PD, Bellman SC, Wagner MJ, Pembrey M, et al. Chen A, et al. Among authors: bellman sc. Am J Med Genet. 1995 Sep 25;58(4):365-70. doi: 10.1002/ajmg.1320580413. Am J Med Genet. 1995. PMID: 8533848

2

X-linked deafness, stapes gushers and a distinctive defect of the inner ear.

Phelps PD, Reardon W, Pembrey M, Bellman S, Luxom L. Phelps PD, et al. Neuroradiology. 1991;33(4):326-30. doi: 10.1007/BF00587816. Neuroradiology. 1991. PMID: 1922747

3

Computed tomography of earpits-deafness syndrome.

Ng YY, Bellman S, Phelps PD. Ng YY, et al. Br J Radiol. 1989 Oct;62(742):947-9. doi: 10.1259/0007-1285-62-742-947. Br J Radiol. 1989. PMID: 2819367 No abstract available.

4

Neuro-otological function in X-linked hearing loss: a multipedigree assessment and correlation with other clinical parameters.

Reardon W, Bellman S, Phelps P, Pembrey M, Luxon LM. Reardon W, et al. Acta Otolaryngol. 1993 Nov;113(6):706-14. doi: 10.3109/00016489309135889. Acta Otolaryngol. 1993. PMID: 8291427

5

Ear-nose-throat abnormalities in the CHARGE association.

Morgan D, Bailey M, Phelps P, Bellman S, Grace A, Wyse R. Morgan D, et al. Arch Otolaryngol Head Neck Surg. 1993 Jan;119(1):49-54. doi: 10.1001/archotol.1993.01880130051006. Arch Otolaryngol Head Neck Surg. 1993. PMID: 8417743

6

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. Acta Otolaryngol. 1996 Jul;116(4):521-7. doi: 10.3109/00016489609137883. Acta Otolaryngol. 1996. PMID: 8831836

7

Mapping of DFN2 to Xq22.

Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M. Tyson J, et al. Hum Mol Genet. 1996 Dec;5(12):2055-60. doi: 10.1093/hmg/5.12.2055. Hum Mol Genet. 1996. PMID: 8968763

8

Clinical and genetic heterogeneity in X-linked deafness.

Reardon W, Middleton-Price HR, Malcolm S, Phelps P, Bellman S, Luxon L, Martin JA, Bumby A, Pembrey ME. Reardon W, et al. Br J Audiol. 1992 Apr;26(2):109-14. doi: 10.3109/03005369209077878. Br J Audiol. 1992. PMID: 1628115

9

A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity.

Reardon W, Middleton-Price HR, Sandkuijl L, Phelps P, Bellman S, Luxon L, Pembrey ME, Malcolm S. Reardon W, et al. Genomics. 1991 Dec;11(4):885-94. doi: 10.1016/0888-7543(91)90011-3. Genomics. 1991. PMID: 1783396

10

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.

Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483

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