Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)

Family History as a Risk Assessment Tool

Number 478

Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

Array Comparative Genomic Hybridization in Prenatal Diagnosis

Number 446

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

Number 442

(Replaces No. 298, August 2004)

Spinal Muscular Atrophy

Number 432

Preimplantation Genetic Screening for Aneuploidy

Number 430

Screening for Tay - Sachs Disease

Number 318

(Reaffirmed 2010, Replaces No. 162, November 1995)