Author/Creator: Butler, M G - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Butler, M G

11. No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD). Issue 11 (1st November 2002)

Authors:: Talebizadeh, Z; Bittel, D C; Miles, J H; Takahashi, N; Wang, C H; Kibiryeva, N; Butler, M G
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 11(2002)
Page Start:: e70
Record Type:: Journal Article
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12. Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism. Issue 5 (28th April 2006)

Authors:: Talebizadeh, Z; Lam, D Y; Theodoro, M F; Bittel, D C; Lushington, G H; Butler, M G
Journal:: Journal of medical genetics
Issue:: Volume 43:Issue 5(2006)
Page Start:: e21
Record Type:: Journal Article
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13. Omphalocele in three generations with autosomal dominant transmission. Issue 3 (1st March 2002)

Authors:: Kanagawa, S L; Begleiter, M L; Ostlie, D J; Holcomb, G; Drake, W; Butler, M G
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 3(2002)
Page Start:: 184
Record Type:: Journal Article
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14. P component in the synovium in rheumatoid and osteoarthritis. Issue 6 (June 1988)

Authors:: Butler, M G; D'Ardenne, A J; Scott, D L
Journal:: Annals of the rheumatic diseases
Issue:: Volume 47:Issue 6(1988)
Page Start:: 463
Record Type:: Journal Article
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15. Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region. Issue 3 (1st March 2002)

Authors:: Butler, M G; Bittel, D; Talebizadeh, Z
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 3(2002)
Page Start:: 202
Record Type:: Journal Article
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16. Rapid technique of DNA-DNA in situ hybridisation on formalin fixed tissue sections using microwave irradiation. Issue 8 (August 1987)

Authors:: Coates, P J; Hall, P A; Butler, M G; D'Ardenne, A J
Journal:: Journal of clinical pathology
Issue:: Volume 40:Issue 8(1987)
Page Start:: 865
Record Type:: Journal Article
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17. Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?. Issue 8 (August 1996)

Authors:: Butler, M G; Mowrey, P
Journal:: Journal of medical genetics
Issue:: Volume 33:Issue 8(1996)
Page Start:: 719
Record Type:: Journal Article
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18. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations. Issue 4 (1st April 2005)

Authors:: Butler, M G; Dasouki, M J; Zhou, X-P; Talebizadeh, Z; Brown, M; Takahashi, T N; Miles, J H; Wang, C H; Stratton, R; Pilarski, R; Eng, C
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 4(2005)
Page Start:: 318
Record Type:: Journal Article
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