TY  - GEN
AU  - Tsai,Ellen A
AU  - Grochowski,Christopher M
AU  - Falsey,Alexandra M
AU  - Rajagopalan,Ramakrishnan
AU  - Wendel,Danielle
AU  - Devoto,Marcella
AU  - Krantz,Ian D
AU  - Loomes,Kathleen M
AU  - Spinner,Nancy B
TI  - Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia
SN  - 1098-1004
PY  - 2016///0301
KW  - Adult
KW  - Alleles
KW  - Biliary Atresia
KW  - diagnosis
KW  - DNA Copy Number Variations
KW  - Facies
KW  - Female
KW  - Genetic Association Studies
KW  - Genotype
KW  - Hepatocyte Nuclear Factor 3-beta
KW  - genetics
KW  - Heterotaxy Syndrome
KW  - Heterozygote
KW  - Humans
KW  - Hypopituitarism
KW  - Infant
KW  - Male
KW  - Pedigree
KW  - Phenotype
KW  - Sequence Analysis, DNA
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1002/humu.22786
ER  -