Ashkenazi Jewish Carrier Testing
Carrier testing for specific inherited diseases, such as cystic fibrosis, Tay-Sachs disease, Canavan disease and familial dysautonomia to individuals of Ashkenazi Jewish descent.

Carrier Testing
Parental blood test that determines if a couple is at increased risk of having a baby with a specific inherited disease, such as Tay-Sachs disease or cystic fibrosis.

Cystic Fibrosis Carrier Testing
Cystic Fibrosis Carrier Testing can help determine if a couple is at risk of having a child with Cystic Fibrosis.

Fragile X Carrier Testing
The fragile X carrier test provides specific information about whether or not individuals are fragile X carriers, and, therefore, about their risks of having a child with fragile X syndrome.

Preimplantation Genetic Screening
Preimplantation Genetic Screening (PGS) through Genzyme Genetics screens embryos for certain chromosome abnormalities prior to transfer into a woman’s uterus.

Spinal Muscular Atrophy Carrier Testing
Parental blood test to see if a couple is at increased risk for giving birth to a child who will be affected with Spinal Muscular Atrophy (SMA).

Ashkenazi Jewish Carrier Testing
Carrier testing for specific inherited diseases, such as cystic fibrosis, Tay-Sachs disease, Canavan disease and familial dysautonomia to individuals of Ashkenazi Jewish descent.

Carrier Testing
Parental blood test that determines if a couple is at increased risk of having a baby with a specific inherited disease, such as Tay-Sachs disease or cystic fibrosis.

Cystic Fibrosis Carrier Testing
Cystic Fibrosis Carrier Testing can help determine if a couple is at risk of having a child with Cystic Fibrosis.

Fragile X Carrier Testing
The fragile X carrier test provides specific information about whether or not individuals are fragile X carriers, and, therefore, about their risks of having a child with fragile X syndrome.

Preimplantation Genetic Screening
Preimplantation Genetic Screening (PGS) through Genzyme Genetics screens embryos for certain chromosome abnormalities prior to transfer into a woman’s uterus.

Spinal Muscular Atrophy Carrier Testing
Parental blood test to see if a couple is at increased risk for giving birth to a child who will be affected with Spinal Muscular Atrophy (SMA).

FirstScreen^®
Maternal serum screening test that screens for Down syndrome and trisomy 18.

IntegratedScreen^SM (first part)
2-part maternal serum screening test that combines results from the 1^st & 2^nd trimester to screen for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

SequentialScreen^SM (first part)
2-part maternal serum screening test that screens for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

SerumIntegratedScreen^SM (first part)
2-part maternal serum screening test that combines results from the 1^st & 2^nd trimester to screen for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

Chorionic Villi Sampling (CVS) Testing
Diagnostic testing for chromosome abnormalities and/or specific inherited diseases.

Ultrasound
Shows images of your developing baby on a monitor.

Ashkenazi Jewish Carrier Testing
Carrier testing for specific inherited diseases, such as cystic fibrosis, Tay-Sachs disease, Canavan disease and familial dysautonomia to individuals of Ashkenazi Jewish descent.

Carrier Testing
Parental blood test that determines if a couple is at increased risk of having a baby with a specific inherited disease, such as Tay-Sachs disease or cystic fibrosis.

Cystic Fibrosis Carrier Testing
Cystic Fibrosis Carrier Testing can help determine if a couple is at risk of having a child with Cystic Fibrosis.

Fragile X Carrier Testing
The fragile X carrier test provides specific information about whether or not individuals are fragile X carriers, and, therefore, about their risks of having a child with fragile X syndrome.

Preimplantation Genetic Screening
Preimplantation Genetic Screening (PGS) through Genzyme Genetics screens embryos for certain chromosome abnormalities prior to transfer into a woman’s uterus.

Spinal Muscular Atrophy Carrier Testing
Parental blood test to see if a couple is at increased risk for giving birth to a child who will be affected with Spinal Muscular Atrophy (SMA).

Afp4^® Screening
Maternal serum screening test that measures certain proteins to screen for Down syndrome, trisomy 18 and open neural tube defects.

IntegratedScreen^SM (second part)
2-part maternal serum screening test that combines results from the 1^st & 2^nd trimester to screen for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

SequentialScreen^SM (second part)
2-part maternal serum screening test that screens for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

SerumIntegratedScreen^SM (second part)
2-part maternal serum screening test that combines results from the 1^st & 2^nd trimester to screen for Down syndrome, trisomy 18 and open neural tube defects, such as spina bifida.

Amniocentesis/Amniotic Fluid Testing
Diagnostic testing for chromosome abnormalities and open neural tube defects, and/or specific inherited diseases.

Ultrasound
Shows images of your developing baby on a monitor.

Ashkenazi Jewish Carrier Testing
Carrier testing for specific inherited diseases, such as cystic fibrosis, Tay-Sachs disease, Canavan disease and familial dysautonomia to individuals of Ashkenazi Jewish descent.

Carrier Testing
Parental blood test that determines if a couple is at increased risk of having a baby with a specific inherited disease, such as Tay-Sachs disease or cystic fibrosis.

Cystic Fibrosis Carrier Testing
Cystic Fibrosis Carrier Testing can help determine if a couple is at risk of having a child with Cystic Fibrosis.

Fragile X Carrier Testing
The fragile X carrier test provides specific information about whether or not individuals are fragile X carriers, and, therefore, about their risks of having a child with fragile X syndrome.

Preimplantation Genetic Screening
Preimplantation Genetic Screening (PGS) through Genzyme Genetics screens embryos for certain chromosome abnormalities prior to transfer into a woman’s uterus.

Spinal Muscular Atrophy Carrier Testing
Parental blood test to see if a couple is at increased risk for giving birth to a child who will be affected with Spinal Muscular Atrophy (SMA).

Amniocentesis/Amniotic Fluid Testing
Diagnostic testing for chromosome abnormalities and open neural tube defects, and/or specific inherited diseases.

Ultrasound
Shows images of your developing baby on a monitor.