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Genomics and other omics tools for enabling Medical Decisions (GOMED)

The GOMED programme aims to provide a platform for clinicians to tap into the rich and varied expertise of CSIR-IGIB in disease genomics to solve clinical problems. The Institute brings to table its pioneering expertise in genomics in the country, demonstrated over almost a decade through the Indian Genome variation project, the sequencing of first Indian personal genome and ongoing clinical genomics efforts in rare and common diseases with a large number of public and private healthcare institutions in the

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Genomics and other omics tools for enabling Medical Decisions (GOMED) | gomed.igib.in Reviews
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The GOMED programme aims to provide a platform for clinicians to tap into the rich and varied expertise of CSIR-IGIB in disease genomics to solve clinical problems. The Institute brings to table its pioneering expertise in genomics in the country, demonstrated over almost a decade through the Indian Genome variation project, the sequencing of first Indian personal genome and ongoing clinical genomics efforts in rare and common diseases with a large number of public and private healthcare institutions in the
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1 search this site
2 about us
3 impact stories
4 genomic tests
5 referral instructions
6 disease information
7 new tests available
8 news and updates
9 partners
10 cerebral cavernous malformations
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search this site,about us,impact stories,genomic tests,referral instructions,disease information,new tests available,news and updates,partners,cerebral cavernous malformations,statistics,why it matters,csir instit,referral statistics,here,by vinod scaria
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Genomics and other omics tools for enabling Medical Decisions (GOMED) | gomed.igib.in Reviews

https://gomed.igib.in

The GOMED programme aims to provide a platform for clinicians to tap into the rich and varied expertise of CSIR-IGIB in disease genomics to solve clinical problems. The Institute brings to table its pioneering expertise in genomics in the country, demonstrated over almost a decade through the Indian Genome variation project, the sequencing of first Indian personal genome and ongoing clinical genomics efforts in rare and common diseases with a large number of public and private healthcare institutions in the

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New Tests Available - Genomics and other omics tools for enabling Medical Decisions (GOMED)

http://gomed.igib.in/new-tests-available

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Genetic testing for Tuberous Sclerosis. Posted Sep 20, 2016, 2:42 AM. By Vinod Scaria [ updated Sep 20, 2016, 2:49 AM. At as part of he...

2

Disease Information - Genomics and other omics tools for enabling Medical Decisions (GOMED)

http://gomed.igib.in/disease-information

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Rare Disease India on Facebook. Genetics and genetic testing of Peutz-Jeghers syndrome. Genetics and genetic testing of Achondroplasia.

3

Genetic screening of Lamellar Icthyosis - Genomics and other omics tools for enabling Medical Decisions (GOMED)

http://gomed.igib.in/new-tests-available/geneticscreeningoflamellaricthyosis

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Genetic screening of Lamellar Icthyosis. Posted Aug 24, 2016, 8:51 PM. By Vinod Scaria [ updated Sep 8, 2016, 7:19 AM.

4

News and Updates - Genomics and other omics tools for enabling Medical Decisions (GOMED)

http://gomed.igib.in/news-and-updates

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Genomics for Clinicians - Jaipur 2016. Posted Jul 20, 2016, 11:39 PM. By Vinod Scaria [ updated Jul 29, 2016, 12:43 AM.

5

Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease - Genomics and other omics tools for enabling Medical Decisions (GOMED)

http://gomed.igib.in/new-tests-available/untitledpost-1

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Posted Aug 8, 2016, 10:16 PM. Nstructions for Referring a patient.

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Initiatives - India | ORD India

http://ordindia.org/resources/initiatives-india

Helpline : 91 8892 555 000. Email : contactus@ordindia.org. History, Vision and Mission. Donate for a Cause. Physicians & Specialists. Genetic Counselling Centres in India. Initiatives – India. Initiatives – Globally. Initiatives – India. Initiatives – India. Birth Defects Registry of India(BDRI). Lysosomal Storage Disorders Supprot Society. Metabolic Errors and Rare Diseases organization. Association for Social and Health Advancement. Alzheimers and Related Disorders Society Of India. Donate for a Cause.

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Publications - Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network

http://guardian.meragenome.com/publications

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. GenoDerma (03-05 Feb 2017, Pune) - Genomics in Clinical Dermatology. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Exome sequencing reve...

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Genomics and other omics tools for enabling Medical Decisions (GOMED)

Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Ute of Genomics and Integrative Biology (CSIR-IGIB). The sequencing of first Indian personal genome. Who benefits from this programme.

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NZOZ GOMED PSZCZYNA

MIEJ PEWNOŚĆ - ZBADAJ SIĘ. Serdeczne życzenia radości i siły płynącej z istoty Świąt Wielkanocnych,. By uśmiech i wiosenny optymizm towarzyszyły Wam każdego dnia. Witamy Państwa na naszej stronie Niepublicznego Zakładu Opieki Zdrowotnej NZOZ Gomed. Przychodnię Centrum Zdrowia Kobiety w Pszczynie. Wykonujemy badania MAMMOGRAFII zarówno w ramach Programów Profilaktycznych jak i Poradni Chorób Piersi. Ensytometryczną, mammograficzną, USG oraz USG Doppler. PORADNIA GINEKOLOGICZNA DLA DZIECI. Rozszczep wargi ...

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