Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

Family History as a Risk Assessment Tool

Number 478

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

Maternal–Fetal Surgery for Myelomeningocele

Number 550

Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

Preconception and Prenatal Carrier Screening for Genetic Diseases in Individuals of Eastern European Jewish Descent

Number 442

(Replaces No. 298, August 2004)

Preimplantation Genetic Screening for Aneuploidy

Number 430

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)