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Leader in Next Gen Sequencing - Fulgent Diagnostics Archive - Fulgent Diagnostics

Specimen Requirements and Logistics. Fulgent Diagnostics also offers Carrier or Mutation Specific testing. Del/Dup is available for all the hereditary tests in our portfolio. Use our Chat feature for quick answers to gene availability, pricing, or anything else we might be able to help you with. Name (click name for details). Zellweger Syndrome NGS Panel. PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6. Xeroderma Pigmentosum NGS Panel. Wolfram Syndrome Comprehensive NGS Panel.

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Fulgent Therapeutics Inc

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Fulgent Therapeutics Inc

Jian Xie

4978 Santa●●●●●●●●●● suite 205

Temp●●●●City , CA, 91780

UNITED STATES

0626●●●●4254
ja●●●●●●@fulgent-therapeutics.com

View this contact

Fulgent Therapeutics Inc

Jian Xie

4978 Santa●●●●●●●●●● suite 205

Temp●●●●City , CA, 91780

UNITED STATES

0626●●●●4254
ja●●●●●●@fulgent-therapeutics.com

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Leader in Next Gen Sequencing - Fulgent Diagnostics Archive - Fulgent Diagnostics | fulgentdiagnostics.com Reviews
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Specimen Requirements and Logistics. Fulgent Diagnostics also offers Carrier or Mutation Specific testing. Del/Dup is available for all the hereditary tests in our portfolio. Use our Chat feature for quick answers to gene availability, pricing, or anything else we might be able to help you with. Name (click name for details). Zellweger Syndrome NGS Panel. PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6. Xeroderma Pigmentosum NGS Panel. Wolfram Syndrome Comprehensive NGS Panel.
<META>
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1 testing info
2 overview
3 fact sheet
4 patient information
5 vus reclassification
6 billing
7 research
8 our company
9 about us
10 accreditation
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Leader in Next Gen Sequencing - Fulgent Diagnostics Archive - Fulgent Diagnostics | fulgentdiagnostics.com Reviews

https://fulgentdiagnostics.com

Specimen Requirements and Logistics. Fulgent Diagnostics also offers Carrier or Mutation Specific testing. Del/Dup is available for all the hereditary tests in our portfolio. Use our Chat feature for quick answers to gene availability, pricing, or anything else we might be able to help you with. Name (click name for details). Zellweger Syndrome NGS Panel. PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6. Xeroderma Pigmentosum NGS Panel. Wolfram Syndrome Comprehensive NGS Panel.

INTERNAL PAGES

fulgentdiagnostics.com fulgentdiagnostics.com
1

Fulgent Diagnostics - Leader in Next Generation Sequencing

http://fulgentdiagnostics.com/test/usher-syndrome-ngs-panel

Usher Syndrome NGS Panel. ABHD12, ADGRV1, CDH23, CIB2, CLRN1, WHRN, MYO7A, PCDH15, PDZD7, USH1C, USH1G, USH2A - 12 genes. Rush / STAT - AVAILABLE. Del / Dup - AVAILABLE. Seq - 81479(5), 81408(2), 81404(2), 81407(3). Del/Dup - 81479(11), 81406. Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in TE buffer) or Buccal Swab or Saliva (kits available upon request). See How to Order.

2

Fulgent Diagnostics - Leader in Next Generation Sequencing

http://fulgentdiagnostics.com/test/wolfram-syndrome-comprehensive-ngs-panel

Wolfram Syndrome Comprehensive NGS Panel. CISD2, WFS1 - 2 genes. Rush / STAT - AVAILABLE. Del / Dup - AVAILABLE. Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in TE buffer) or Buccal Swab or Saliva (kits available upon request). See How to Order.

3

Fulgent Diagnostics - Leader in Next Generation Sequencing

http://fulgentdiagnostics.com/test/thyroid-cancer-ngs-panel

Thyroid Cancer NGS Panel. BRAF, HRAS, KRAS, MUTYH, NRAS, PTEN, RET, SDHB, SDHD, TP53 - 10 genes. Rush / STAT - AVAILABLE. Del / Dup - AVAILABLE. Seq - 81406(2), 81404(2), 81405(3), 81311, 81321, 81401. Del/Dup - 81479(9), 81323. Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in TE buffer) or Buccal Swab or Saliva (kits available upon request). See How to Order.

4

Fulgent Diagnostics - Leader in Next Generation Sequencing

http://fulgentdiagnostics.com/testing/patient-information

Browse or search for the test you are interested in. Edit the test if needed. Add desired test to your cart. Go to your cart. Login to the portal and checkout. Complete the ordering process and submit your order. Print out Test Requisition Form (TRF). Send in the specimen along with the TRF. Specimen Requirements and Logistics:. Fulgent Diagnostics accepts various types of specimens. The information below will provide a guide for which type might be best for your situation. Saliva / Buccal Swab:. If you ...

5

Fulgent Diagnostics - Leader in Next Generation Sequencing

http://fulgentdiagnostics.com/test/tetrahydrofolate-metabolism-ngs-panel

Tetrahydrofolate Metabolism NGS Panel. DHFR, FOLR1, FPGS, MTHFD1, MTHFD1L, MTHFS, PTS, SHMT1, SLC19A1 - 9 genes. Rush / STAT - AVAILABLE. Del / Dup - AVAILABLE. Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in TE buffer) or Buccal Swab or Saliva (kits available upon request). See How to Order.

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geneticobesity.com geneticobesity.com

Find a Diagnostic Testing Lab - The Genetic Obesity ProjectThe Genetic Obesity Project

http://geneticobesity.com/resources/diagnostic-testing-pomc-lepr-deficiency

About the Genetic Obesity Project. About Rare Genetic Disorders of Obesity. About the MC4 Pathway. Find a Treatment Referral Center. Find a Diagnostic Testing Lab. Patients & Healthcare Professionals:. Join the effort to identify people. I am a Healthcare Professional. I am a Patient or Caregiver. Find a Diagnostic Testing Lab. Find a Treatment Referral Center. Find a Diagnostic Testing Lab. Find a Diagnostic Testing Lab. Baylor Miraca Genetics Laboratories. POMC, PCSK1, LEPR. Test codes: 6860, 6861).

andreasscherer.com andreasscherer.com

Genetics Archives - The Point

http://andreasscherer.com/category/genetics

Be Fast Or Be Gone. Andreas Scherer on business, management and life. Golden Helix: Empowering Precision Medicine. March 31, 2016. Recently, I was interviewed by CIOReview on Golden Helix. I gave them an overview of our strategy as well as our entire solution stack. Please read the entire article here. Filed Under: Big Picture. Tagged With: Andreas Scherer. Announcing VSWarehouse Golden Helix’s Data Warehouse Solution for genomic data. January 21, 2016. Why did we build VSWarehouse? Read all about it in.

alportsyndrome.org alportsyndrome.org

Genetic Testing Labs - Alport Syndrome

http://alportsyndrome.org/resources/genetic-testing-labs

Contact Us: 480.800.3510. I am a patient/caregiver. What is Alport Syndrome? Ask The Experts Series. Hear From the Experts. About Alport Syndrome Foundation. Message from the Board. I am a Physician. 2017 Request for Proposals. Paul Silver Tribute Award. Paul Silver Tribute Award Previous Winners. Support & Connect. Fundraising & Events. Annual Campaign for Healthy Kidneys. I am a patient/caregiver. What is Alport Syndrome? Ask The Experts Series. Hear From the Experts. About Alport Syndrome Foundation.

bohring-opitz.org bohring-opitz.org

Bohring-Opitz Syndrome / ASXL1 – Bohring-Opitz Syndrome

https://bohring-opitz.org/bosasxl1

A worldwide exchange of information and awareness. Bohring-Opitz Syndrome / ASXL1. Map “Children with BOS”. Other Cases which are compared with BOS. High 5 for BOS. Bohring-Opitz Syndrome / ASXL1. Bohring-Opitz Syndrome (BOS) is a very rare congenital disorder. In 2015, there are less than 60 children in the world, diagnosed with this syndrome and presented in medical articles (Russell, B. et al. 2015). One Cause of BOS:. The research by Hoischen et al. (2011) results in a third important conclusion:.

andreasscherer.com andreasscherer.com

VarSeq Archives - The Point

http://andreasscherer.com/tag/varseq

Be Fast Or Be Gone. Andreas Scherer on business, management and life. Announcing VSWarehouse Golden Helix’s Data Warehouse Solution for genomic data. January 21, 2016. 8220;So, why do we launch a new data warehouse product? Why did we build VSWarehouse? According to Grand View Market Research. Read all about it in. Filed Under: Genetic Research. Tagged With: Genetic Data Warhouse. Clinical Reporting comes to VarSeq. September 17, 2015. 8220;The next release of VarSeq. Read more from Our 2 SNPs… here.

senaissance.com senaissance.com

Senaissance

http://www.senaissance.com/Clients.aspx

Senaissance Software boasts of many happy clients across industries from different lines of businesses. Each business has its own requirement and we, at Senaissance, understand this and customize technological solutions to satisfy their diverse needs after analyzing their business processes and core objectives. Our long term and steadfast association with our clientele reflects on our commitment to supreme service delivery and our expertise to channelize our innovation into substantial solutions.

saidsupport.org saidsupport.org

Finding a Diagnosis

http://saidsupport.org/patient-resources/finding-a-diagnosis

Systemic Autoinflammatory Disease (SAID) Support. Welcome to the Autoinflammatory Alliance blog for discussing all things involving awareness, advocacy, care and thriving with SAID. Skip to primary content. Skip to secondary content. New Name Same Mission and Goals. What Does Our Logo Symbolize? NLRC4-Associated Macrophage Activation Syndrome-Like Illness. Cryopyrin-Associated Periodic Syndromes (CAPS). Action & Advocacy. Tips and Resources for Patients (Adults and Children) on Biological Medications.

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Fulgent Inter-Net Publishing and Provisioning. For finest reception and transmission of your digitized bits, use Fulgent. Brand inter-networked computational units. To contact us, send an electronic post to our inter-net mailbox. Our address is information AT fulgent DOT net. Please use proper electronic postage.

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Leader in Next Gen Sequencing - Fulgent Diagnostics Archive - Fulgent Diagnostics

Specimen Requirements and Logistics. Fulgent Diagnostics also offers Carrier or Mutation Specific testing. Del/Dup is available for all the hereditary tests in our portfolio. Use our Chat feature for quick answers to gene availability, pricing, or anything else we might be able to help you with. Name (click name for details). Zellweger Syndrome NGS Panel. PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6. Xeroderma Pigmentosum NGS Panel. Wolfram Syndrome Comprehensive NGS Panel.

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