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

Author/Creator Bourrouillou, G

1. Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome. Issue 4 (1st April 2002)

Authors:: De Mas, P; Chassaing, N; Chaix, Y; Vincent, M-C; Julia, S; Bourrouillou, G; Calvas, P; Bieth, E
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 4(2002)
Page Start:: e17
Record Type:: Journal Article
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2. Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations. Issue 9 (5th September 2003)

Authors:: Luciani, J J; de Mas, P; Depetris, D; Mignon-Ravix, C; Bottani, A; Prieur, M; Jonveaux, P; Philippe, A; Bourrouillou, G; de Martinville, B; Delobel, B; Vallee, L; Croquette, M-F; Mattei, M-G
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 9(2003)
Page Start:: 690
Record Type:: Journal Article
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3. Towards a suggestive facial dysmorphism in adenylosuccinate lyase deficiency?. Issue 6 (1st June 2002)

Authors:: Holder-Espinasse, M; Marie, S; Bourrouillou, G; Ceballos-Picot, I; Nassogne, M-C; Faivre, L; Amiel, J; Munnich, A; Vincent, M-F; Cormier-Daire, V
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 6(2002)
Page Start:: 440
Record Type:: Journal Article
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