Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.
Bogani, Debora
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. [electronic resource] - Proceedings of the National Academy of Sciences of the United States of America Aug 2005 - 12477-82 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0027-8424
10.1073/pnas.0500584102 doi
Animals
Anophthalmos--genetics
Brain--abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 6--genetics
Congenital Abnormalities--genetics
Craniofacial Abnormalities--genetics
Female
Genes, Lethal
Genes, Recessive
Genetic Testing--methods
Heart Defects, Congenital--genetics
Humans
Kidney--abnormalities
Male
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Mutant Strains
Multigene Family
Mutation
Phenotype
Species Specificity
Syndrome
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. [electronic resource] - Proceedings of the National Academy of Sciences of the United States of America Aug 2005 - 12477-82 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0027-8424
10.1073/pnas.0500584102 doi
Animals
Anophthalmos--genetics
Brain--abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 6--genetics
Congenital Abnormalities--genetics
Craniofacial Abnormalities--genetics
Female
Genes, Lethal
Genes, Recessive
Genetic Testing--methods
Heart Defects, Congenital--genetics
Humans
Kidney--abnormalities
Male
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Mutant Strains
Multigene Family
Mutation
Phenotype
Species Specificity
Syndrome