Kết quả tìm kiếm - M‐C De Blois
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1
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders Bằng M-L Jacquemont, Damien Sanlaville, Richard Redon, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M Le Merrer, D. Héron, M‐C De Blois, M Prieur, Michel Vekemans, N P Carter, A Munnich, Laurence Colleaux, Anne Philippe
Được phát hành 2006Artigo -
2
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech Bằng Céline Bonnet, Joris Andrieux, Mylène Béri‐Dexheimer, B. Leheup, O. Boute, S. Manouvrier, B Delobel, H. Copin, Aline Receveur, M Mathieu, G. Thiriez, C. Le Caignec, A. David, M. C. de Blois, Valérie Malan, Anne Philippe, Valérie Cormier‐Daire, Laurence Colleaux, E. Flori, Hélène Dollfus, V. Pelletier, Christel Thauvin‐Robinet, A. Masurel-Paulet, L. Faivre, Marc Tardieu, Nadia Bahi‐Buisson, Patrick Callier, Francine Mugneret, Patrick Edery, Philippe Jonveaux, Damien Sanlaville
Được phát hành 2010Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Bioinformatics
Biology
Chromosome
Comparative genomic hybridization
Copy-number variation
Gene
Genetics
Genome
Abnormality
Autism
Autism spectrum disorder
Chromosomal Abnormality
Computational biology
Disease gene identification
Exome sequencing
Gene duplication
Gene expression
Gene family
Genetic counseling
Genetic heterogeneity
Hypotonia
Karyotype
Medicine
Microarray
Microdeletion syndrome
Phenotype
Psychiatry
RefSeq
Segmental duplication
Speech delay