TY  - GEN
AU  - de Pontual,Loïc
AU  - Yao,Evelyn
AU  - Callier,Patrick
AU  - Faivre,Laurence
AU  - Drouin,Valérie
AU  - Cariou,Sandra
AU  - Van Haeringen,Arie
AU  - Geneviève,David
AU  - Goldenberg,Alice
AU  - Oufadem,Myriam
AU  - Manouvrier,Sylvie
AU  - Munnich,Arnold
AU  - Vidigal,Joana Alves
AU  - Vekemans,Michel
AU  - Lyonnet,Stanislas
AU  - Henrion-Caude,Alexandra
AU  - Ventura,Andrea
AU  - Amiel,Jeanne
TI  - Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans
SN  - 1546-1718
PY  - 2011///1121
KW  - Animals
KW  - Chromosomes, Human, Pair 13
KW  - genetics
KW  - Databases, Genetic
KW  - Duodenal Obstruction
KW  - Embryo, Mammalian
KW  - Esophageal Atresia
KW  - Eyelids
KW  - abnormalities
KW  - Female
KW  - Gene Deletion
KW  - Germ-Line Mutation
KW  - Haploinsufficiency
KW  - Humans
KW  - Intellectual Disability
KW  - Limb Deformities, Congenital
KW  - Male
KW  - Mice
KW  - Mice, Inbred C57BL
KW  - Mice, Knockout
KW  - MicroRNAs
KW  - Microcephaly
KW  - Models, Animal
KW  - Multigene Family
KW  - Musculoskeletal Development
KW  - Pedigree
KW  - Polymerase Chain Reaction
KW  - Tracheoesophageal Fistula
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ng.915
ER  -