TY  - GEN
AU  - Radhakrishna,Uppala
AU  - Nath,Swapan K
AU  - McElreavey,Ken
AU  - Ratnamala,Uppala
AU  - Sun,Celi
AU  - Maiti,Amit K
AU  - Gagnebin,Maryline
AU  - Béna,Frédérique
AU  - Newkirk,Heather L
AU  - Sharp,Andrew J
AU  - Everman,David B
AU  - Murray,Jeffrey C
AU  - Schwartz,Charles E
AU  - Antonarakis,Stylianos E
AU  - Butler,Merlin G
TI  - Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele
SN  - 1468-6244
PY  - 2012///0810
KW  - Chromosome Duplication
KW  - Chromosomes, Human, Pair 1
KW  - Comparative Genomic Hybridization
KW  - DNA Copy Number Variations
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Genome-Wide Association Study
KW  - Haplotypes
KW  - Hernia, Umbilical
KW  - genetics
KW  - Humans
KW  - Lod Score
KW  - Male
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmedgenet-2012-100826
ER  -