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newbornscreening.info - Expanded Newborn Screening Using New Technologies, Financial, Ethical, Legal and Social Issues (FELSI)

newbornscreening.info - Expanded Newborn Screening Using New Technologies, Financial, Ethical, Legal and Social Issues (FELSI)

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Baby's First Test | Newborn Screening | Baby Health
Baby's First Test | Newborn Screening | Baby Health


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newenglandconsortium.org newenglandconsortium.org           
New England Consortium of Metabolic Programs
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counsyl.com counsyl.com           
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galactosemia.org

galactosemia.org galactosemia.org           
Galactosemia Foundation
We connect families affected by galactosemia, and support networking efforts between clinicians and researchers.


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fodsupport.org fodsupport.org           
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scid.net

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Severe Combine Immune Deficiency
SCID, Severe Combined Immunodeficiency, is a primary immune deficiency. The defining characteristic is usually a severe defect in both the T- & B-lymphocyte systems. This usually results in the onset of one or more serious infections within the first few months of life. These infections are usually serious, and may even be life threatening, they […]


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caresfoundation.org

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genedx.com

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medicalhomeportal.org

medicalhomeportal.org medicalhomeportal.org           
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The domain name adagen.com is for sale
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Organic Acidemia Association - we care for the rare
Welcome to the Organic Acidemia AssociationVisit our blog to find the latest OAA news, meet our kids, and find helpful resources.Learn MoreWe Are a Parent-Led CommunityOrganic Acidemia Association is a non-profit organization on a mission to empower families with knowledge and resources for organic acidemia metabolic disorders.Learn More Previous slide Next slide We are parents,…


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newbornscreening.on.ca

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invitae.com

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Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources.


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pku.com

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Personalized support for people living with phenylketonuria (PKU). Get the latest information about the disease, its symptoms, and managing blood Phe levels.



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adhb.govt.nz

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canpku.org

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