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Results 1–19 of 19
Title Date
1.

Screening for Tay - Sachs Disease

Number 318

(Reaffirmed 2014, Replaces No. 162, November 1995)

October 2005

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2.

Perinatal Risks Associated With Assisted Reproductive Technology

Number 324

(Reaffirmed 2007)

November 2005

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3.

Umbilical Cord Blood Banking

Number 399

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

February 2008

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4.

Direct-to-Consumer Marketing of Genetic Testing

Number 409

June 2008

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5.

Ethical Issues in Genetic Testing

Number 410

June 2008

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6.

Preimplantation Genetic Screening for Aneuploidy

Number 430

(Reaffirmed 2014)

March 2009

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7.

Spinal Muscular Atrophy

Number 432

May 2009

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8.

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

Number 442

(Reaffirmed 2014, Replaces No. 298, August 2004)

October 2009

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9.

Maternal Phenylketonuria

Number 449

(Replaces No. 230, January 2000)

December 2009

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10.

Carrier Screening for Fragile X Syndrome

Number 469

(Replaces No. 338, June 2006)

October 2010

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11.

Family History as a Risk Assessment Tool

Number 478

March 2011

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12.

Update on Carrier Screening for Cystic Fibrosis

Number 486

(Replaces No. 325, December 2005)

April 2011

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13.

Pharmacogenetics

Number 488

May 2011

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14.

Personalized Genomic Testing for Disease Risk

Number 527

(Reaffirmed 2014)

June 2012

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15.

Noninvasive Prenatal Testing for Fetal Aneuploidy

Number 545

December 2012

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16.

Maternal–Fetal Surgery for Myelomeningocele

Number 550

January 2013

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17.

Von Willebrand Disease in Women

Number 580

(Replaces No. 451, December 2009)

December 2013

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18.

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis

Number 581

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

December 2013

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19.

Newborn Screening and the Role of the Obstetrician-Gynecologist

Number 616

(Replaces Committee Opinion Number 481, March 2011)

January 2015

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