Array Comparative Genomic Hybridization in Prenatal Diagnosis

Number 446

Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

Direct-to-Consumer Marketing of Genetic Testing

Number 409

Ethical Issues in Genetic Testing

Number 410

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

Newborn Screening

Number 481

(Replaces No. 393, December 2007)

Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

Perinatal Risks Associated With Assisted Reproductive Technology

Number 324

(Reaffirmed 2007)

Personalized Genomic Testing for Disease Risk

Number 527

Pharmacogenetics

Number 488

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

Screening for Tay - Sachs Disease

Number 318

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

Spinal Muscular Atrophy

Number 432

Umbilical Cord Blood Banking

Number 399

(Reaffirmed 2012, Replaces No. 183, April 1997)

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)

Von Willebrand Disease in Women

Number 451