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Results 1–9 of 9
Title Date
1.

Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

October 2010

PDF Format
2.

Family History as a Risk Assessment Tool

Number 478

March 2011

PDF Format
3.

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

December 2009

PDF Format
4.

Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

December 2012

PDF Format
5.

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
6.

Screening for Tay - Sachs Disease

Number 318

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

October 2005

PDF Format
7.

Spinal Muscular Atrophy

Number 432

May 2009

PDF Format
8.

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
9.

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)

April 2011

PDF Format