Author/Creator: Lench, N J - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lench, N J

1. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). Issue 2 (February 1998)

Authors:: Lench, N J; Markham, A F; Mueller, R F; Kelsell, D P; Smith, R J; Willems, P J; Schatteman, I; Capon, H; Van De Heyning, P J; Van Camp, G
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 2(1998)
Page Start:: 151
Record Type:: Journal Article
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2. A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22. Issue 12 (December 1997)

Authors:: Campbell, D A; McHale, D P; Brown, K A; Moynihan, L M; Houseman, M; Karbani, G; Parry, G; Janjua, A H; Newton, V; al-Gazali, L; Markham, A F; Lench, N J; Mueller, R F
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 12(1997)
Page Start:: 1015
Record Type:: Journal Article
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3. Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease. Issue 4 (1st April 2003)

Authors:: Negoro, K; McGovern, D P B; Kinouchi, Y; Takahashi, S; Lench, N J; Shimosegawa, T; Carey, A; Cardon, L R; Jewell, D P; van Heel, D A
Journal:: Gut
Issue:: Volume 52:Issue 4(2003)
Page Start:: 541
Record Type:: Journal Article
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4. Evidence for a common mutation in hereditary pancreatitis. Issue 2 (April 1998)

Authors:: Bell, S M; Bennett, C; Markham, A F; Lench, N J
Journal:: Journal of clinical pathology
Issue:: Volume 51:Issue 2(1998)
Page Start:: 115
Record Type:: Journal Article
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5. Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1. Issue 8 (August 1997)

Authors:: Brown, K A; al-Gazali, L I; Moynihan, L M; Lench, N J; Markham, A F; Mueller, R F
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 8(1997)
Page Start:: 685
Record Type:: Journal Article
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