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Jump to: C | G | R
Number of items: 5.

C

Cohen, M; Francis, M; Coffey, R; Bellman, S; Pembrey, ME; Luxon, LM; (1997) Vestibular findings in pedigree with autosomal recessive non-syndromic hearing loss. In: Book of Abstracts.

Cohen, M; Francis, M; Coffey, R; Pembrey, ME; Luxon, LM; (1997) Abnormal audiograms and elevated acoustic reflex thresholds in obligate carriers of autosomal recessive non-syndromic hearing loss. ACTA OTO-LARYNGOL , 117 (3) 337 - 342.

G

Gausden, E; Coyle, B; Armour, JAL; Coffey, R; Grossman, A; Fraser, GR; ... Trembath, R; + view all (1997) Pendred syndrome: Evidence for genetic homogeneity and further refinement of linkage. J MED GENET , 34 (2) 126 - 129.

Gilbert, HL; Buxton, JL; Chan, CTJ; McKay, T; Cottrell, S; Ramsden, S; ... Malcolm, S; + view all (1997) Counselling dilemmas associated ith the molecular characterisation of two Angelman syndrome families. Journal of Medical Genetics , 34 651 - 655.

R

Reardon, W; Coffey, R; Pembrey, ME; Lucas, D; Harrop-Griffiths, K; Phelps, PD; ... Trembath, R; + view all (1997) Pitfalls in practice, diagnosis and misdiagnosis in Pendred Syndrome. J AUDIOLOGICAL MEDICINE , 6 (1) 1 - 9.

This list was generated on Sun Aug 24 06:43:40 2014 BST.