TY  - GEN
AU  - Itsara,Andy
AU  - Vissers,Lisenka E L M
AU  - Steinberg,Karyn Meltz
AU  - Meyer,Kevin J
AU  - Zody,Michael C
AU  - Koolen,David A
AU  - de Ligt,Joep
AU  - Cuppen,Edwin
AU  - Baker,Carl
AU  - Lee,Choli
AU  - Graves,Tina A
AU  - Wilson,Richard K
AU  - Jenkins,Robert B
AU  - Veltman,Joris A
AU  - Eichler,Evan E
TI  - Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing
SN  - 1537-6605
PY  - 2012///0531
KW  - Base Sequence
KW  - Chromosome Breakpoints
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 17
KW  - genetics
KW  - Comparative Genomic Hybridization
KW  - methods
KW  - DNA Copy Number Variations
KW  - Haplotypes
KW  - Homologous Recombination
KW  - Humans
KW  - Molecular Sequence Data
KW  - Segmental Duplications, Genomic
KW  - Sequence Analysis, DNA
KW  - Smith-Magenis Syndrome
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2012.02.013
ER  -