Brochure and handouts related to genetic testing options available prior and during pregnancy

Brochures and Handouts

Below are handouts and brochures that can be freely used by anyone. They are designed for providers to give to their patients when topics such as carrier screening, amniocentesis, CVS, or cell-free DNA screening (also known as NIPT) are discussed.

Many brochures and handouts come from the genetic testing laboratory performing the test. While many labs have great resources for patients, there can be concern for commercial bias. The below are general factsheets without lab branding.

Prenatal Testing

Genetic testing options prior to pregnancy including carrier screening, personal diagnosis testing, and chromosomal analysis such as karyotype..

Brochure: Genetic Testing Prior to Pregnancy

This brochure discusses what is carrier screening and how it can be helpful. It includes what to consider if you are a carrier of a genetic condition.

Brochure: Carrier Screening

Amniocentesis handout

Handout: Amniocentesis

cell-free DNA screening, noninvasive prenatal testing, nipt, nips handout

Handout: Cell-free DNA Screening

Prenatal whole exome sequencing is a new option available in pregnancy that is able to assess for numerous genes of the pregnancy.

Handout: Prenatal Whole Exome Sequencing (WES)

genetic testing options available in pregnancy including carrier screening, screening for chromosomal conditions, and diagnostic testing such as karyotype and microarray after either an amniocentesis or CVS procedure

Brochure: Genetic Testing in Pregnancy

What to expect from Genetic Counseling. There are different kinds of genetic counseling including oncology, pediatric, adult, and prenatal. This brochure focuses on reproductive genetic counseling which includes both prenatal and preconception.

Brochure: What to Expect from Genetic Counseling?

with a focus on reproductive genetic counseling

environmental exposure impact to reproductive health

Handout: Environmental Exposure Impact to Reproductive Health

Chorionic villi sampling (CVS) handout

Handout: Chorionic Villi Sampling (CVS)

multiple marker screening handout

Handout: Multiple Marker Screening

Diagnostic genetic testing in pregnancy includes FISH, Karyotype, Microarray, and gene panels. These testing options are available after a patient either undergoes a diagnostic procedure such as CVS or amniocentesis.

Brochure: Diagnostic Testing in Pregnancy-What are the Genetic Testing Options?

This brochure discusses what is a chromosome and the type of chromosomal testing including microarray and karyotype.

Brochure: Chromosomal Analysis (karyotype and microarray)

designed for adult patients undergoing chr analysis

Preimplantation Genetic Testing

What is preimplantation genetic testing for aneuploidy or chromosomal abnormalities (PGT-A)

Handout: Preimplantation Genetic Testing-Aneuploidy (PGT-A)

What is preimplantation genetic testing for structural rearrangements (PGT-SR)

Handout: Preimplantation Genetic Testing-Structural Rearrangements (PGT-SR)

what to expect for preimplantation genetic testing for monogenic conditions (PGT-M)

Handout: What to Expect PGT-M

Preimplantation genetic testing for monogenic conditions (PGT-M) eligibility can vary based on the clinical indication and technical aspects. Not every family will have an indication for PGT-M.

Handout: PGT-M Eligibility- SMA Edition

What is preimplantation genetic testing for monogenic conditions (PGT-M)

Handout: Preimplantation Genetic Testing-Monogenic (PGT-M)

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