Silver-Russell Syndrome Testing Kit – Fits Medical Genetics Laboratories (Replaces GTR000331016.5)
Silver-Russell Syndrome Testing Kit – Fits Medical Genetics Laboratories (Replaces GTR000331016.5) is backordered and will ship as soon as it is back in stock.
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Worry-free returns
Worry-free returns
You may return most new, unopened items within 7 days of delivery for a full refund. We'll also pay the return shipping costs if the return is a result of our error (you received an incorrect or defective item, etc.).
You should expect to receive your refund within four weeks of giving your package to the return shipper, however, in many cases you will receive a refund more quickly. This time period includes the transit time for us to receive your return from the shipper (5 to 10 business days), the time it takes us to process your return once we receive it (3 to 5 business days), and the time it takes your bank to process our refund request (5 to 10 business days).
If you need to return an item, simply login to your account, view the order using the "Complete Orders" link under the My Account menu and click the Return Item(s) button. We'll notify you via e-mail of your refund once we've received and processed the returned item.
Delivery and Shipping
Delivery and Shipping
Free standard shipping on all orders under 1 KG
Silver-Russell Syndrome Testing Kit – Fits Medical Genetics Laborat...
Product Details
This laboratory testing kit is designed for diagnosing Silver-Russell Syndrome (RSS), a rare genetic disorder characterized by intrauterine and postnatal growth restriction, relative macrocephaly, a triangular face, and body asymmetry. This Silver-Russell Syndrome Testing Kit analyzes chromosome 11p15 and UPD7 regions to aid in diagnosis. It replaces GTR000331016.5.
This kit serves as a direct replacement for interchange numbers GTR000331016.1, GTR000331016.2, GTR000331016.3, GTR000331016.4, and GTR000331016.5.
Technical Specs
- Product Type
- Clinical Genetic Test
- Test Purpose
- Diagnosis; Mutation Confirmation
- Target Population
- Patients with suspected Silver-Russell Syndrome
- Testing Method
- Molecular Genetics - Deletion/duplication analysis: High resolution aCGH; Methylation analysis: Quantitative methylation-specific PCR; Uniparental disomy study (UPD)
- Specimens Accepted
- Amniocytes, Amniotic fluid, Cord blood, Fetal blood, Fibroblasts, Isolated DNA, Peripheral (whole) blood, Saliva, Skin
- Chromosomal Regions Analyzed
- 11p15, UPD7
- Clinical Validity
- Analysis of chromosome 11p15 can detect methylation errors and abnormal copy number in approximately 50% of affected individuals. Maternal uniparental disomy for chromosome 7 occurs in about 10% of affected individuals. Chromosomal aberrations on 11p15 or chromosome 7 can be observed in 1-2% of RSS patients.
- Technical Specifications
- Tests performed entirely in-house; Proficiency testing performed using intra-laboratory methods
- Product Dimensions
- 10.0" L x 17.0" W x 0.1" H
What’s in the Box
- 1 x Test Kit for Silver-Russell Syndrome Testing (GTR000331016.5)
Ordering & Sample Submission
Ordering and sample submission must be performed by a qualified health care provider. Please refer to the "INSTRUCTIONS FOR SAMPLE SUBMISSION" page provided in the laboratory's paperwork for detailed guidance. The laboratory can only accept contact from health care providers; patients and families should discuss testing options with their physician or genetic counselor.
Troubleshooting & FAQ
Who is eligible to order this test?
This test can be ordered by a Genetic Counselor, Health Care Provider, In-State Patients, Licensed Physician, Nurse Practitioner, Out-of-State Patients, Physician Assistant, or Registered Nurse.
What conditions does this test help diagnose?
This test is designed to detect genetic markers associated with Silver-Russell syndrome 1 (C5393125) and Silver-Russell syndrome due to an imprinting defect of 11p15 (C5680916).
Is pre- or post-test genetic counseling required?
No, neither pre-test nor post-test genetic counseling is required by the laboratory, though it is often recommended as best practice in genetic testing.
Is informed consent required?
Informed consent requirements are based on applicable state law. Please consult your local regulations.
What contacts and resources are available from the lab?
The lab can only be contacted by healthcare providers. Patients should consult their provider. For more information, you can visit the lab's website or the specific test page.
What is the difference between OEM and aftermarket parts?
This listing is an aftermarket replacement (not OEM). It is built to OEM-level specifications with comparable materials. The product is manufactured in an ISO 9002 facility and is batch-inspected for consistency and quality.
What are your shipping speed and cost?
We ship worldwide quickly—typical transit is 5–15 days. Standard shipping is free; expedited options appear at checkout where available.
What is the warranty and return policy?
This product is covered by a 1-year warranty against manufacturing defects under normal use. If any issues arise, please contact our support team with your order details. Returns are accepted within our standard window for unused items in their original condition. See our policy page or reach out for instructions.
Safety & Important Info
- Verify all test specifications against your clinical requirements. If anything differs—even if your patient appears to be a candidate—do not order.
- This is an aftermarket replacement, not an OEM component.
- For clinical diagnostic use only. Must be ordered and administered by a qualified healthcare professional.
About Sea Sierra
- Pro-Grade Standards — We supply marine parts engineered to OEM-level tolerances and tested for real-world conditions.
- Fast Global Fulfillment — Free standard delivery to most regions in 5–15 days.
- Manufacturer-Direct Value — Fair pricing without compromising on materials or QC.
Payment & Security
Payment methods
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