Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Journal article published in 2023 by
Mythily Ganapathi 
,
Matsuoka Ls,
Leticia S. Matsuoka,
Michael March,
Dong Li,
Elly Brokamp,
Sara Benito-Sanz,
Susan M. White,
Katherine Lachlan,
Priyanka Ahimaz,
Anshuman Sewda,
Lisa Bastarache,
Amanda Thomas-Wilson,
Stoler Jm,
Joan M. Stoler
and other authors.
,
Matsuoka Ls,
Leticia S. Matsuoka,
Michael March,
Dong Li,
Elly Brokamp,
Sara Benito-Sanz,
Susan M. White,
Katherine Lachlan,
Priyanka Ahimaz,
Anshuman Sewda,
Lisa Bastarache,
Amanda Thomas-Wilson,
Stoler Jm,
Joan M. Stoler
and other authors.
