Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

(2013) Ellen A Croonen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic assessment following increased nuchal translucency and normal karyotype

(2011) Eugene Pergament et al.   PRENATAL DIAGNOSIS

Prenatal features of Noonan syndrome: prevalence and prognostic value

(2011) G. Baldassarre et al.   PRENATAL DIAGNOSIS

RAS-MAPK pathway disorders: important causes of congenital heart disease, feeding difficulties, developmental delay and short stature

(2010) E. M. M. B. Wright et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Noonan syndrome: Prenatal diagnosis in a woman carrying aPTPN11gene mutation

(2010) Norma Celia González-Huerta et al.   Journal of Maternal-Fetal & Neonatal Medicine

Polyhydramnios, fetal overgrowth, and macrocephaly: Prenatal ultrasound findings of Costello syndrome

(2009) Laura P. Smith et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

PTPN11analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings

(2009) KA Lee et al.   CLINICAL GENETICS

Spontaneous Resolution of Cystic Hygroma and Hydrops in a Fetus with Noonan’s Syndrome

(2009) Asuka Kiyota et al.   FETAL DIAGNOSIS AND THERAPY

Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia

(2009) Angela E. Lin et al.   PRENATAL DIAGNOSIS

Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D

(2008) Hideo Kuniba et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The cardiofaciocutaneous syndrome: prenatal findings in two patients

(2007) I. Witters et al.   PRENATAL DIAGNOSIS