TY  - GEN
AU  - Jehee,Fernanda S
AU  - de Oliveira,Valdirene T
AU  - Gurgel-Giannetti,Juliana
AU  - Pietra,Rafaella X
AU  - Rubatino,Fernando V M
AU  - Carobin,Natália V
AU  - Vianna,Gabrielle S
AU  - de Freitas,Mariana L
AU  - Fernandes,Karla S
AU  - Ribeiro,Beatriz S V
AU  - Brüggenwirth,Hennie T
AU  - Ali-Amin,Roza
AU  - White,Janson J
AU  - Akdemir,Zeynep C
AU  - Jhangiani,Shalini N
AU  - Gibbs,Richard A
AU  - Lupski,James R
AU  - Varela,Monica C
AU  - Koiffmann,Célia
AU  - Rosenberg,Carla
AU  - Carvalho,Cláudia M B
TI  - Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins
SN  - 1552-4833
PY  - 2017///1130
KW  - Adolescent
KW  - Base Sequence
KW  - genetics
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 15
KW  - Comparative Genomic Hybridization
KW  - Exome
KW  - Facies
KW  - Female
KW  - Humans
KW  - Hyperventilation
KW  - diagnosis
KW  - Intellectual Disability
KW  - Obesity
KW  - Pathology, Molecular
KW  - Phenotype
KW  - Prader-Willi Syndrome
KW  - Transcription Factor 4
KW  - Twins, Monozygotic
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.38315
ER  -