Congenital Anomalies

Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders

Three-dimensional models of the segmented human fetal brain generated by magnetic resonance imaging

Early prenatal detection of Bardet-Biedl syndrome in a case with postaxial polydactyly and hyperechoic kidneys confirmed by next generation sequencing

A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects

SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly

Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9

59th Annual Meeting of the Japanese Society of Teratology (JST) & 13th World Congress of the International Cleft Lip and Palate Foundation (ICPF) CLEFT2019 Nagoya, Japan July 26- 2019 Abstracts

Induction of a thoracolumbar supernumerary rib in rat developmental toxicity studies: A short discussion on the critical window

A next generation sequencing custom gene panel designed to distinguish isolated polydactyly from syndromic polydactyly during prenatal diagnosis

Induction of a thoracolumbar supernumerary rib in rat developmental toxicity studies: A short discussion on the critical window