Author/Creator: Strain, L - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Strain, L

1. A novel atypical 22q11.2 distal deletion in father and son. Issue 10 (1st October 2002)

Authors:: Garcia-Miñaur, S; Fantes, J; Murray, R S; Porteous, M E M; Strain, L; Burns, J E; Stephen, J; Warner, J P
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 10(2002)
Page Start:: e62
Record Type:: Journal Article
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2. Confirmation of prenatal diagnosis of cystic fibrosis by DNA typing of fetal tissues. Issue 2 (February 1988)

Authors:: Curtis, A; Strain, L; Mennie, M; Brock, D J
Journal:: Journal of medical genetics
Issue:: Volume 25:Issue 2(1988)
Page Start:: 79
Record Type:: Journal Article
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3. Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus. Issue 3 (March 1996)

Authors:: Jouet, M; Strain, L; Bonthron, D; Kenwrick, S
Journal:: Journal of medical genetics
Issue:: Volume 33:Issue 3(1996)
Page Start:: 248
Record Type:: Journal Article
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4. Fragile X syndrome with FMR1 and FMR2 deletion. Issue 7 (1st July 1999)

Authors:: Moore, S J; Strain, L; Cole, G F; Miedzybrodzka, Z; Kelly, K F; Dean, J C S
Journal:: Journal of medical genetics
Issue:: Volume 36:Issue 7(1999)
Page Start:: 565
Record Type:: Journal Article
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5. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22. Issue 7 (July 1997)

Authors:: Strain, L; Wright, A F; Bonthron, D T
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 7(1997)
Page Start:: 535
Record Type:: Journal Article
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6. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family. Issue 6 (1st June 2001)

Authors:: Kovács, G G; Ertsey, C; Majtényi, C; Jelencsik, I; László, L; Flicker, H; Strain, L; Szirmai, I; Budka, H
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 70:Issue 6(2001)
Page Start:: 802
Record Type:: Journal Article
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7. Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2. Issue 4 (April 1998)

Authors:: Porteous, M E; Strain, L; Logie, L J; Herd, R M; Benton, E C
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 4(1998)
Page Start:: 336
Record Type:: Journal Article
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8. Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. Issue 8 (August 1997)

Authors:: FitzPatrick, D R; Strain, L; Thomas, A E; Barr, D G; Todd, A; Smith, N M; Scobie, W G
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 8(1997)
Page Start:: 666
Record Type:: Journal Article
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9. The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts. Issue 11 (22nd March 2005)

Authors:: Fremeaux-Bacchi, V; Kemp, E J; Goodship, J A; Dragon-Durey, M-A; Strain, L; Loirat, C; Deng, H-W; Goodship, T H J
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 11(2005)
Page Start:: 852
Record Type:: Journal Article
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