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

Noonan syndrome and clinically related disorders

(2011) Marco Tartaglia et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Whole genome amplification in preimplantation genetic diagnosis

(2011) Ying-ming Zheng et al.   Journal of Zhejiang University-SCIENCE B

Prenatal features of Noonan syndrome: prevalence and prognostic value

(2011) G. Baldassarre et al.   PRENATAL DIAGNOSIS

Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype

(2010) Simone Martinelli et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

A restricted spectrum of NRAS mutations causes Noonan syndrome

(2009) Ion C Cirstea et al.   NATURE GENETICS

Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia

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

Electrocardiography in Noonan syndromePTPN11 gene mutation—phenotype characterization

(2008) Ellen A. Croonen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A