TY  - GEN
AU  - Pergande,Matthias
AU  - Motameny,Susanne
AU  - Özdemir,Özkan
AU  - Kreutzer,Mona
AU  - Wang,Haicui
AU  - Daimagüler,Hülya-Sevcan
AU  - Becker,Kerstin
AU  - Karakaya,Mert
AU  - Ehrhardt,Harald
AU  - Elcioglu,Nursel
AU  - Ostojic,Slavica
AU  - Chao,Cho-Ming
AU  - Kawalia,Amit
AU  - Duman,Özgür
AU  - Koy,Anne
AU  - Hahn,Andreas
AU  - Reimann,Jens
AU  - Schoner,Katharina
AU  - Schänzer,Anne
AU  - Westhoff,Jens H
AU  - Schwaibold,Eva Maria Christina
AU  - Cossee,Mireille
AU  - Imbert-Bouteille,Marion
AU  - von Pein,Harald
AU  - Haliloglu,Göknur
AU  - Topaloglu,Haluk
AU  - Altmüller,Janine
AU  - Nürnberg,Peter
AU  - Thiele,Holger
AU  - Heller,Raoul
AU  - Cirak,Sebahattin
TI  - The genomic and clinical landscape of fetal akinesia
SN  - 1530-0366
PY  - 2021///0203
KW  - Adolescent
KW  - Adult
KW  - Arthrogryposis
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - DNA Copy Number Variations
KW  - Female
KW  - Fetal Diseases
KW  - Genetic Predisposition to Disease
KW  - Guanine Nucleotide Exchange Factors
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Muscular Diseases
KW  - RNA-Binding Proteins
KW  - Ryanodine Receptor Calcium Release Channel
KW  - Trans-Activators
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/s41436-019-0680-1
ER  -