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Page 1
X chromosome and infantile autism.
Petit E, Hérault J, Raynaud M, Cherpi C, Perrot A, Barthélémy C, Lelord G, Müh JP. Petit E, et al. Biol Psychiatry. 1996 Sep 15;40(6):457-64. doi: 10.1016/0006-3223(96)85270-X. Biol Psychiatry. 1996. PMID: 8879465 Clinical Trial.
Catecholaminergic metabolism and autism.
Martineau J, Hérault J, Petit E, Guérin P, Hameury L, Perrot A, Mallet J, Sauvage D, Lelord G, Müh JP. Martineau J, et al. Among authors: petit e. Dev Med Child Neurol. 1994 Aug;36(8):688-97. doi: 10.1111/j.1469-8749.1994.tb11911.x. Dev Med Child Neurol. 1994. PMID: 7914177
Serotonin and autism: biochemical and molecular biology features.
Hérault J, Petit E, Martineau J, Cherpi C, Perrot A, Barthélémy C, Lelord G, Müh JP. Hérault J, et al. Among authors: petit e. Psychiatry Res. 1996 Nov 1;65(1):33-43. doi: 10.1016/0165-1781(96)02882-x. Psychiatry Res. 1996. PMID: 8953659
Genetic markers in autism: association study on short arm of chromosome 11.
Hérault J, Martineau J, Petit E, Perrot A, Sauvage D, Barthélémy C, Mallet J, Müh JP, Lelord G. Hérault J, et al. Among authors: petit e. J Autism Dev Disord. 1994 Apr;24(2):233-6. doi: 10.1007/BF02172100. J Autism Dev Disord. 1994. PMID: 7913707 No abstract available.
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.
Hovnanian A, Rochat A, Bodemer C, Petit E, Rivers CA, Prost C, Fraitag S, Christiano AM, Uitto J, Lathrop M, Barrandon Y, de Prost Y. Hovnanian A, et al. Among authors: petit e. Am J Hum Genet. 1997 Sep;61(3):599-610. doi: 10.1086/515495. Am J Hum Genet. 1997. PMID: 9326325 Free PMC article.
756 results