Menu

carriermap

Determine your risk of passing on over 300 genetic diseases to your future child.

80% of children born with a genetic condition have no family history of that disease. CarrierMap is an expanded carrier screen that can help you plan for a healthy family.

CarrierMap is recommended for people who are planning a family or early in pregnancy.

chromomap

Gain insight into the health of your pregnancy with one simple blood test.

Chromosome abnormalities such as Down syndrome impact over 1 in 107 pregnancies. ChromoMap is a non-invasive prenatal screen to assess risk for these conditions.

ChromoMap is available for women who are at least 10 weeks pregnant.

fertilitymap

Contribute to a first-of-its-kind study on the links between genomics and infertility.

1 in 6 couples are impacted by infertility. Through large-scale research, FertilityMap seeks to optimize fertility treatment, helping more families achieve successful pregnancies.

Participation in FertilityMap is currently only open to patients of partner clinics.

genetic counseling

Navigate the complicated world of genomics with help from Recombine’s expert genetic counselors.

Recombine is focused on comprehensive patient care and offers detailed genetic counseling pre- and post-test to help give the most complete picture of your family’s risk.

Recombine genetic counseling is available alongside CarrierMap and ChromoMap at no additional charge.

Connect with Recombine

Phone: 855-OUR-GENES (855-687-4363)

Location: 1140 Broadway, Suite 1100, New York 10001

×

Disease List

ChromoMap screens for aneuploidies and microdeletions that can significantly impact a child’s health and quality of life or cause adverse pregnancy outcomes.

Standard Panel

The standard panel screens for three trisomies. A trisomy is an extra copy of an entire chromosome.

  • Trisomy 21 (Down Syndrome)
  • Trisomy 13 (Patau Syndrome)
  • Trisomy 18 (Edwards Syndrome)

Optional Add-Ons*

Trisomies 9 and 16
These trisomies are associated with an increased risk of miscarriage

  • Trisomy 9
  • Trisomy 16

Microdeletions
A microdeletion is a change in which a small segment of genetic material is missing from a specific chromosome.

  • 22q11.2 (DiGeorge syndrome, Velocardiofacial Syndrome)
  • 1p36 Deletion Syndrome
  • 15q11.2 (Angelman/Prader Willi Syndrome)
  • 5p- (Cri du Chat Syndrome)
  • 4p- (Wolf-Hirschhorn Syndrome)

Sex Aneuploidies
Sex aneuploidies are missing or extra copies of the sex chromosomes, X and Y. If sex aneuploidies are screened for, the fetal sex will be identified.

  • Monosomy X (Turner Syndrome)
  • XXX (Triple X Syndrome)
  • XXY (Klinefelter Syndrome)
  • XYY (Jacob Syndrome)
  • Fetal Sex Identification

*Add-on panels available for singleton pregnancies only.