Müh JP - Search Results

1

Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder.

Vourc'h P, Petit E, Müh JP, Andres C, Bienvenu T, Beldjord C, Chelly J, Barthélémy C. Vourc'h P, et al. Among authors: muh jp. Am J Med Genet. 2002 Mar 1;108(2):164-7. doi: 10.1002/ajmg.10210. Am J Med Genet. 2002. PMID: 11857568 No abstract available.

2

Association study of the NF1 gene and autistic disorder.

Mbarek O, Marouillat S, Martineau J, Barthélémy C, Müh JP, Andres C. Mbarek O, et al. Among authors: muh jp. Am J Med Genet. 1999 Dec 15;88(6):729-32. Am J Med Genet. 1999. PMID: 10581497

3

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Eur J Hum Genet. 2001 Jul;9(7):556-8. doi: 10.1038/sj.ejhg.5200660. Eur J Hum Genet. 2001. PMID: 11464249

4

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

Vourc'h P, Martin I, Marouillat S, Adrien JL, Barthélémy C, Moraine C, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Neurosci Lett. 2003 Feb 27;338(2):115-8. doi: 10.1016/s0304-3940(02)01338-1. Neurosci Lett. 2003. PMID: 12566166

5

Autism and genetics: clinical approach and association study with two markers of HRAS gene.

Hérault J, Petit E, Martineau J, Perrot A, Lenoir P, Cherpi C, Barthélémy C, Sauvage D, Mallet J, Müh JP. Hérault J, et al. Among authors: muh jp. Am J Med Genet. 1995 Aug 14;60(4):276-81. doi: 10.1002/ajmg.1320600404. Am J Med Genet. 1995. PMID: 7485261

6

Association study with two markers of a human homeogene in infantile autism.

Petit E, Hérault J, Martineau J, Perrot A, Barthélémy C, Hameury L, Sauvage D, Lelord G, Müh JP. Petit E, et al. Among authors: muh jp. J Med Genet. 1995 Apr;32(4):269-74. doi: 10.1136/jmg.32.4.269. J Med Genet. 1995. PMID: 7643354 Free PMC article.

7

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. Among authors: muh jp. Biol Psychiatry. 1996 Sep 15;40(6):457-64. doi: 10.1016/0006-3223(96)85270-X. Biol Psychiatry. 1996. PMID: 8879465 Clinical Trial.

8

X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.

Gendrot C, Ronce N, Raynaud M, Ayrault AD, Dourlens J, Castelnau P, Muh JP, Chelly J, Moraine C. Gendrot C, et al. Among authors: muh jp. Am J Med Genet. 1999 Apr 23;83(5):411-8. Am J Med Genet. 1999. PMID: 10232754

9

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: muh jp. Psychiatry Res. 1996 Nov 1;65(1):33-43. doi: 10.1016/0165-1781(96)02882-x. Psychiatry Res. 1996. PMID: 8953659

10

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

Vourc'h P, Dessay S, Mbarek O, Marouillat Védrine S, Müh JP, Andres C. Vourc'h P, et al. Among authors: muh jp. Brain Res Dev Brain Res. 2003 Sep 10;144(2):159-68. doi: 10.1016/s0165-3806(03)00167-6. Brain Res Dev Brain Res. 2003. PMID: 12935913

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