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Results 1–16 of 16
Title Date
1.

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis

Number 581

(Replaces No. 446, November 2009) (See also Practice Bulletin No. 88)

December 2013

PDF Format
2.

Maternal–Fetal Surgery for Myelomeningocele

Number 550

January 2013

PDF Format
3.

Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

December 2012

PDF Format
4.

Personalized Genomic Testing for Disease Risk

Number 527

June 2012

PDF Format
5.

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)

April 2011

PDF Format
6.

Newborn Screening

Number 481

(Replaces No. 393, December 2007)

March 2011

PDF Format
7.

Family History as a Risk Assessment Tool

Number 478

March 2011

PDF Format
8.

Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

October 2010

PDF Format
9.

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

December 2009

PDF Format
10.

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

Number 442

(Replaces No. 298, August 2004)

October 2009

PDF Format
11.

Spinal Muscular Atrophy

Number 432

May 2009

PDF Format
12.

Ethical Issues in Genetic Testing

Number 410

June 2008

PDF Format
13.

Direct-to-Consumer Marketing of Genetic Testing

Number 409

June 2008

PDF Format
14.

Umbilical Cord Blood Banking

Number 399

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

February 2008

PDF Format
15.

Perinatal Risks Associated With Assisted Reproductive Technology

Number 324

(Reaffirmed 2007)

November 2005

PDF Format
16.

Screening for Tay - Sachs Disease

Number 318

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

October 2005

PDF Format