J. Müh

发表

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

C. Barthélémy, P. Vourc'h, C. Andres, 2001, European Journal of Human Genetics.

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist

C. Andres, P. Corcia, P. Couratier, 2002, Neurology.

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis

C. Andres, P. Corcia, W. Camu, 2002, Annals of neurology.

Three Novel Point Mutations in the Keratinocyte Transglutaminase (TGK) Gene in Lamellar Ichthyosis: Significance for Mutant Transcript Level, TGK Immunodetection and Activity

C. Bodemer, M. Lathrop, Y. Barrandon, 1997, European journal of human genetics : EJHG.

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

C. Barthélémy, P. Vourc'h, C. Andres, 2002, American journal of medical genetics.

Serotonin and autism: Biochemical and molecular biology features

C. Barthélémy, J. Martineau, G. Lelord, 1996, Psychiatry Research.

Characterization of human follicle-stimulating hormone binding to human granulosa cells by an immunoenzymological method.

Y. Combarnous, F. Perrotin, J. Lansac, 1992, Analytical biochemistry.

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder

C. Barthélémy, P. Vourc'h, C. Andres, 2003, Neuroscience Letters.

Possible association of c-harvey-ras-1 (HRAS-1) marker with autism

M. Leboyer, J. Mallet, C. Barthélémy, 1993, Psychiatry Research.

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

J. Mallet, C. Barthélémy, J. Martineau, 1995, American journal of medical genetics.

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

C. Barthélémy, J. Martineau, G. Lelord, 1995, Journal of medical genetics.

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

P. Vourc'h, C. Andres, O. Mbarek, 2003, Brain research. Developmental brain research.

Association study of the NF1 gene and autistic disorder.

C. Barthélémy, J. Martineau, C. Andres, 1999, American journal of medical genetics.

X chromosome and infantile autism

C. Barthélémy, G. Lelord, M. Raynaud, 1996, Biological Psychiatry.

CATECHOLAMINERGIC METABOLISM AND AUTISM

J. Mallet, P. Guérin, G. Lelord, 1994, Developmental medicine and child neurology.

Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine‐rich repeat domain, not its glycosylphosphatidyl‐inositol anchor

P. Vourc'h, C. Andres, T. Moreau, 2003, Journal of neurochemistry.

Genetic markers in autism: Association study on short arm of chromosome 11

C. Barthélémy, J. Martineau, G. Lelord, 1994, Journal of autism and developmental disorders.