TY  - GEN
AU  - Bogani,Debora
AU  - Willoughby,Catherine
AU  - Davies,Jennifer
AU  - Kaur,Kulvinder
AU  - Mirza,Ghazala
AU  - Paudyal,Anju
AU  - Haines,Heather
AU  - McKeone,Richard
AU  - Cadman,Matthew
AU  - Pieles,Guido
AU  - Schneider,Jürgen E
AU  - Bhattacharya,Shoumo
AU  - Hardy,Andrea
AU  - Nolan,Patrick M
AU  - Tripodis,Nikos
AU  - Depew,Michael J
AU  - Chandrasekara,Ramya
AU  - Duncan,Gimara
AU  - Sharpe,Paul T
AU  - Greenfield,Andy
AU  - Denny,Paul
AU  - Brown,Steve D M
AU  - Ragoussis,Jiannis
AU  - Arkell,Ruth M
TI  - Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
SN  - 0027-8424
PY  - 2005///1013
KW  - Animals
KW  - Anophthalmos
KW  - genetics
KW  - Brain
KW  - abnormalities
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 6
KW  - Congenital Abnormalities
KW  - Craniofacial Abnormalities
KW  - Female
KW  - Genes, Lethal
KW  - Genes, Recessive
KW  - Genetic Testing
KW  - methods
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Kidney
KW  - Male
KW  - Mice
KW  - Mice, Inbred C3H
KW  - Mice, Inbred C57BL
KW  - Mice, Mutant Strains
KW  - Multigene Family
KW  - Mutation
KW  - Phenotype
KW  - Species Specificity
KW  - Syndrome
N1  - Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1073/pnas.0500584102
ER  -