M. Blois

发表

The character of 1,1,1-trichloro-2,2-bis-(p-chlorophenyl)ethane. Resistance in mouse L 5178 Y lymphoma cells.

J. Spalding, E. Ford, D. Lane, 1971, Biochemical pharmacology.

Toxicity of metabolites produced by the "Alternaria".

J. Spalding, D. Harvan, R. Pero, 1973, Environmental health perspectives.

Profiling Lgals 9 Splice Variant Expression at the Fetal-Maternal Interface : Implications in Normal and Pathological Human Pregnancy 1

Sandra, B. Klapp, N. Freitag, 2013 .

Expression Embryos Reveal an Asymmetric Pattern of Follicular Fluid , and Preimplantation Analysis of HLA-G in Maternal Plasma

Sandra, R. Cherry, I. Morrison, 2008 .

Isolation of the toxin, altenuisol, from the fungus, auct.

D. Harvan, R. Pero, M. Blois, 1973 .

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH

A. Munnich, A. Bernheim, M. Vekemans, 2013, Clinical genetics.

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

R Redon, D Sanlaville, L Colleaux, 2006, Journal of Medical Genetics.

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype

A. Munnich, A. Aurias, S. Romana, 2001, Clinical genetics.

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

A. Munnich, L. Faivre, S. Jacquemont, 2002, Journal of medical genetics.

Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid.

Y. Ville, J. Bernard, M. Vekemans, 2013, European journal of medical genetics.

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation

A. Munnich, S. Lyonnet, M. Vekemans, 2002, Journal of medical genetics.

Automated fluorescent genotyping detects 10 % of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation

C. Ozilou, M. L. Merrer, M. Blois, 2002 .

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

L. Faivre, S. Jacquemont, M. Vekemans, 2002, Journal of medical genetics.

Toxicity of metabolites produced by the "Alternaria".

J. Spalding, D. Harvan, R. Pero, 1973, Environmental health perspectives.

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

L. Faivre, H. Dollfus, P. Jonveaux, 2010, Journal of Medical Genetics.

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

A. Munnich, M. Vekemans, M. D. de Blois, 2003, Journal of medical genetics.