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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Pediatric Genetic Testing" (30 stories)

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Baylor Genetics to Showcase How Genome Sequencing is Advancing Pediatric Care at the 2026 Child Neurology Society Annual Meeting
Lead StoryThe Manila Timesgeneral
4h ago

Baylor Genetics to Showcase How Genome Sequencing is Advancing Pediatric Care at the 2026 Child Neurology Society Annual Meeting

<a href="https://news.google.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?oc=5" target="_blank">Baylor Genetics to Showcase How Genome Sequencing is Advancing Pediatric Care at the 2026 Child Neurology Society Annual Meeting</a>  <font color="#6f6f6f">The Manila Times</font>

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Search Results for "Pediatric Genetic Testing"

Updated every 3 minutes via FreeNewsApi, GNews, Currents API & Google News

29 stories displayed
PCM GENES: Pediatric HCM, Severe LVH and Gene Variants
American College of Cardiologygeneral

PCM GENES: Pediatric HCM, Severe LVH and Gene Variants

<a href="https://news.google.com/rss/articles/CBMiiAFBVV95cUxQdFZjRDhnczA0WDItMHUzMTdtV05FaGVLWG9FUE9qZk9zX3YyVkhWekRFQl9sYmdpZ2tHQ2ZFcUJDYmtXVFdPeVBmOXBVeEhhQkdLcEd3U0w3RDM0UzczNTBNRENJeWtMOTZmLU9jN1pGbjFSZkVmdnJzYkU1ZHJmdlJSdnh6czRC?oc=5" target="_blank">PCM GENES: Pediatric HCM, Severe LVH and Gene Variants</a>  <font color="#6f6f6f">American College of Cardiology</font>

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Interdisciplinary management and genetic evaluation of pediatric cancer predisposition syndromes: a retrospective cohort study
Naturegeneral

Interdisciplinary management and genetic evaluation of pediatric cancer predisposition syndromes: a retrospective cohort study

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1EWVVrSHhIT1QzZjBDa3c2b043QklvYzFNTkQ5WDdWUGh4eFhsYXJ0SHJIOVVMNTlfb1B3V1RDTFFmanlkVkItdHdsQkJkUDB0TGlmelBXMjExUkVRVnlF?oc=5" target="_blank">Interdisciplinary management and genetic evaluation of pediatric cancer predisposition syndromes: a retrospective cohort study</a>  <font color="#6f6f6f">Nature</font>

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Q&A: Dr. Vivian Chang discusses genetic testing, treatment for pediatric cancer
Daily Bruingeneral

Q&A: Dr. Vivian Chang discusses genetic testing, treatment for pediatric cancer

<a href="https://news.google.com/rss/articles/CBMirgFBVV95cUxNRUpyNHg2b1didGpKSEpTOW1pYnllZ2Z2U0toOWdSLTNtdWRCU3BScHpBWllnUzIwSHhtTHI3amdXLVZabWxXMTRucko5aWtWNGNhcFVHeFN2Z2VrZHUyYWdXUkM0X29XSmwyQjVjdUdkUFdPYkgxUnNOOXh2QWhiZWw0N2loWGhNWmdWVHhjR2tXTU9UMWszZDlrODRGMklDQ1lUU2pNT3hPdFNWOFE?oc=5" target="_blank">Q&A: Dr. Vivian Chang discusses genetic testing, treatment for pediatric cancer</a>  <font color="#6f6f6f">Daily Bruin</font>

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New Breath and Genetic Testing Project Aims to Diagnose Asthma in Young Children
Respiratory Therapytech

New Breath and Genetic Testing Project Aims to Diagnose Asthma in Young Children

<a href="https://news.google.com/rss/articles/CBMiywFBVV95cUxPdFlGb056NVNVWlFRNVRzQ0RnNDQzTXV1V3M0cUlQbDlQdzhBNTlrdFVIeXg5LUd0UjByR200TDFTbFJFMU5jSlJMQjVXLUVwQkRadzRqYklxR19iRUt0OHloWFZiVnJ5QlB6OWZXa01fZWRaU2VhdlZkdUhKQWJ2bnQxLU0xbmVHSlBmenJKOGZKNTFfWFROd2dISUlyd05ZbzE3ZFc3enhydTBveEF4RVNwSU9iVEp5YWN6dU1OU08wOEhOV3BlSDhEMA?oc=5" target="_blank">New Breath and Genetic Testing Project Aims to Diagnose Asthma in Young Children</a>  <font color="#6f6f6f">Respiratory Therapy</font>

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Whole Genome Sequencing Diagnoses 47% Neurological Pediatric Cases
Inside Precision Medicinegeneral

Whole Genome Sequencing Diagnoses 47% Neurological Pediatric Cases

<a href="https://news.google.com/rss/articles/CBMixAFBVV95cUxNS1VjWE90RXJTbnZWQVZVZlYtc1dHQTZWTHIzMlg2YU1ZMGhvaVFvZXFnU1FnZ0VSRGhrbmxUTndOZjhjZlQ4ZExhOG50cjhYdTk2c2RHcGlEUjR1S0hkR0NIcnV4T0xRUXNNZzRWNzBQREpleW8yTlplM2hCOFRFbkJFMy12YkYzZzVrWUZCQUtVYy14VjV4OTI0UzVZY2ZTNGVpWWczekxFZ2JxdlZTVWVQbmt0ak41QTZ6T1M0b0pER2hz?oc=5" target="_blank">Whole Genome Sequencing Diagnoses 47% Neurological Pediatric Cases</a>  <font color="#6f6f6f">Inside Precision Medicine</font>

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Genetic clues help reveal kids’ cancer risk
UKNowgeneral

Genetic clues help reveal kids’ cancer risk

<a href="https://news.google.com/rss/articles/CBMihAFBVV95cUxNMGdQa01CWUlBSmhTVWhRbkF3eXNGVjFucndZRmswMGNzWHo2UXdhcGhFUUs4alNib2R6NUM5NEdjLXc1XzNZdENxX0hfbTZnRmR0QzBMMVRTQkx5WDZhbnZuZFo1cTAxc184WDhIUER1aGVJUDY3Z2dTMUlXc1o0NF82djc?oc=5" target="_blank">Genetic clues help reveal kids’ cancer risk</a>  <font color="#6f6f6f">UKNow</font>

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GeneDx Introduces Easy Order at AAP 2026 to Simplify Genomic Testing in Everyday Pediatric Care
Business Wiregeneral

GeneDx Introduces Easy Order at AAP 2026 to Simplify Genomic Testing in Everyday Pediatric Care

<a href="https://news.google.com/rss/articles/CBMi5wFBVV95cUxQMU5yQm1qXzFDVTRfV1hXblp2czNYcU9pNTB5dTVBb2lzamlfS240d0Ria01ad0lUbE9yZjdVc3JFUVYzNmVsOFd0eWIyUmtPLTVWc1RHQlVLblVfWDh0YlBVQUdiTW1LbWp1TVdZdUJaX1dhWW5DYUpmaUkzOFFURkpYNW5FVjE1TTZ4RkN1R0haSWw4OEt1UE1kZlBqUHpjUUZsNGpvQTk2TDdyZGY2TjVWdnlsRF9uaXdQTUV5TTcxaWFRUW9NZGlCTmRBMzU0WmMzQktvZlFJV1A1UHdPdVR2TmpaRDg?oc=5" target="_blank">GeneDx Introduces Easy Order at AAP 2026 to Simplify Genomic Testing in Everyday Pediatric Care</a>  <font color="#6f6f6f">Business Wire</font>

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Beyond Wall Thickness: Defining Genotype-Phenotype Relationships in Pediatric Hypertrophic Cardiomyopathy
JACC Journalsgeneral

Beyond Wall Thickness: Defining Genotype-Phenotype Relationships in Pediatric Hypertrophic Cardiomyopathy

<a href="https://news.google.com/rss/articles/CBMiYEFVX3lxTE1uX25vUWlMZzRFcmZzQlJDRW1ScFB3SFZhX2RNaHB5SUpVcmxSWDZYYXhRLVJHUjBoZllFMm41N1ZMTHIyXzlHTnNHLXBpaExCbWd2bldZYW9PQzYyRUdNbQ?oc=5" target="_blank">Beyond Wall Thickness: Defining Genotype-Phenotype Relationships in Pediatric Hypertrophic Cardiomyopathy</a>  <font color="#6f6f6f">JACC Journals</font>

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Largest Pediatric Pancreatitis Genetics Study Identifies Risk Variants Tied to Disease Progression
Research Horizonsgeneral

Largest Pediatric Pancreatitis Genetics Study Identifies Risk Variants Tied to Disease Progression

<a href="https://news.google.com/rss/articles/CBMi2wFBVV95cUxOR0d3S2lXdnlQX3lzaV9uYVhtamJEVExOOVk3cGtjM29mSHBOVHVZZ1dLc2pLX0k2eHAzcDBJdmQ0RUV1QWZWaHhNUnFhckl6VGNfMjU4Qm80cnFtSTBneEZYSjNyVlA0RkdyVVhlVzU5YTlFRVp5QlVOZzhTSF9xUXRRWTZ1dVZHN2JCdVVIcjE5Y2xQLWRSVjRVc3JQbHJfQlVMVjQ1bmVaWUQ3OW5iY29kcUlhcF9FOUJmYjlSU1BXb3JuMzhSN0d5RTIzVjVpZXpfSXllTEhuUUE?oc=5" target="_blank">Largest Pediatric Pancreatitis Genetics Study Identifies Risk Variants Tied to Disease Progression</a>  <font color="#6f6f6f">Research Horizons</font>

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New international guideline advances genetic testing for childhood short stature
Children's Nationalgeneral

New international guideline advances genetic testing for childhood short stature

<a href="https://news.google.com/rss/articles/CBMiygFBVV95cUxPMVBaOXk0VUU4WmxDdG5LUXZLZ0twbFZWUkdFZFFNdU9aaGtwV3BtdllEdTdEZ0JYY2pPOHBkTEZ4VU5iS3NKbUZTZmFMU3JIVmZQaVNucXpZN2Z1dUZhdHd2YWszTVVpdVd6QUU2dVBQRHZQTlh1bDExR1IySUtLcllCUU5EQXhQQTFsMU4wNnZ4RUNPaUh1QXhFSHBna3I4WGdJVjdWaDFxdkRnU0VLZHJhc3RjVWNtdDVaZ2txNmYwSTNZRVJicFFn?oc=5" target="_blank">New international guideline advances genetic testing for childhood short stature</a>  <font color="#6f6f6f">Children's National</font>

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Children’s Hospital Los Angeles Study Explores How Genetic Testing May Inform SSRI Prescribing for Pediatric Patients | Newswise
Newswisegeneral

Children’s Hospital Los Angeles Study Explores How Genetic Testing May Inform SSRI Prescribing for Pediatric Patients | Newswise

<a href="https://news.google.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?oc=5" target="_blank">Children’s Hospital Los Angeles Study Explores How Genetic Testing May Inform SSRI Prescribing for Pediatric Patients | Newswise</a>  <font color="#6f6f6f">Newswise</font>

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Simple Workflow Changes Double Genetic Testing Referrals for Children With Hearing Loss
University of Miamigeneral

Simple Workflow Changes Double Genetic Testing Referrals for Children With Hearing Loss

<a href="https://news.google.com/rss/articles/CBMitgFBVV95cUxQTWh6bTNmaXRRZGpHbVFLM01QWWE0OFhpcUk1SjNCeHpBYlN4aXN6ZjAtR1pSY2h1VnpSQ1B0bGlGTmt1VGtPNXFscHpsV2kxVHdrVWNQTjNJTXVkS25peWh0NHNJem1jRjFNRlhKWDhscHlNTkZZQTdNeXE1Mm1GeHduY1NCMkU0VlJldmZuZDBFOEdGa3diM29CS2Fub1ZhSlhnWk93REhTMkdHdXowbC1zUGZmdw?oc=5" target="_blank">Simple Workflow Changes Double Genetic Testing Referrals for Children With Hearing Loss</a>  <font color="#6f6f6f">University of Miami</font>

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Genetic Testing Could Be Helpful in Pediatric ADHD
Psychiatric Timesgeneral

Genetic Testing Could Be Helpful in Pediatric ADHD

<a href="https://news.google.com/rss/articles/CBMikgFBVV95cUxPeDdvN2ZtU2Nzc0gzV3BTb1JOVnEwVzZQcGIzaC1wNWgyVlpTUmlLUE1Kdm5EdU03N2lac1NQWUNjOWhlQVhjNTZ3VkFkYWlPV1p2THVENFpvZHNYVTE0SmU5b25hcHRMeUpZNzZOb05LUjFjVTJLemhRYy1DUWhTUEE5OUthUWh0NzI0OVBkZTdndw?oc=5" target="_blank">Genetic Testing Could Be Helpful in Pediatric ADHD</a>  <font color="#6f6f6f">Psychiatric Times</font>

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Using AI to help physicians diagnose rare genetic diseases affecting children
OpenAItech

Using AI to help physicians diagnose rare genetic diseases affecting children

<a href="https://news.google.com/rss/articles/CBMiakFVX3lxTE5POTdmdEl1dGVqVHZ5d05NV2VqaUIyQ3ExVjgyUkVMaWtOSm5ZZ0RJdGJxNzVRdEZCWG14bnZDSEc3bkhwbXNhZjZBaHNaUXVndDE2YV9SNl85LWh2dEFvVVJRQ1pJdTBWRGc?oc=5" target="_blank">Using AI to help physicians diagnose rare genetic diseases affecting children</a>  <font color="#6f6f6f">OpenAI</font>

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Pathogenic germline variations and cancer risks in pediatric patients referred for genetic testing
Naturegeneral

Pathogenic germline variations and cancer risks in pediatric patients referred for genetic testing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE8ybUd3WFExdTVNRDdWS2k1VURpUVZxOUNJZW1xR2pqa2pLall4eXdKbUNWTDQwNUo0TkN4T0t1WXk3emFXbi1Bai1Ed05nR21oMEphUjN4cDVnWEJIMWIw?oc=5" target="_blank">Pathogenic germline variations and cancer risks in pediatric patients referred for genetic testing</a>  <font color="#6f6f6f">Nature</font>

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Pathogenic germline variants identify elevated cancer risk in pediatric patients referred for genetic testing
Naturegeneral

Pathogenic germline variants identify elevated cancer risk in pediatric patients referred for genetic testing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9POWZTb0REck9ZTzZtOGtaUlVJallDNnlEUUhKSzJVNXlIaUF4d2MzOERGWWRDVHpVQ0N3bE1vX0l5RXEtWEo1ck5Sb1pQV1ppUU4zY2RuRWgyR0lqV1VZ?oc=5" target="_blank">Pathogenic germline variants identify elevated cancer risk in pediatric patients referred for genetic testing</a>  <font color="#6f6f6f">Nature</font>

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Diagnostic yield and genetic landscape of rare pediatric diseases in Vietnam identified by exome sequencing
Naturegeneral

Diagnostic yield and genetic landscape of rare pediatric diseases in Vietnam identified by exome sequencing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBWWGI1SDEyTmNLSWVXcXBtQ3VpWGs2WUVBNENZS0p2cXBackFQc2dLRlQ1S3VDNUdsNmNOYW9zYVZkdm5tT195QWctR2RNQVJnS212NU5BZmNJaDE5ajI0?oc=5" target="_blank">Diagnostic yield and genetic landscape of rare pediatric diseases in Vietnam identified by exome sequencing</a>  <font color="#6f6f6f">Nature</font>

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Novel genetic variants and atypical phenotypes in pediatric progressive familial intrahepatic cholestasis
Naturegeneral

Novel genetic variants and atypical phenotypes in pediatric progressive familial intrahepatic cholestasis

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5ZNnJUTHduVHlkd1djLTNCSU9yRnZic2NNTFk3NGxsZlRrYjBIVG45VkhsVzlTZ1RQNURaYmkzNlpNRzNHTkx2dzBDWHYwSXl1Smp4UnJyVEd0cDJkMmtj?oc=5" target="_blank">Novel genetic variants and atypical phenotypes in pediatric progressive familial intrahepatic cholestasis</a>  <font color="#6f6f6f">Nature</font>

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Citywide implementation of a rapid whole-genome sequencing program for critically ill pediatric patients
Naturegeneral

Citywide implementation of a rapid whole-genome sequencing program for critically ill pediatric patients

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9LYlhMbC0xSXFvb25TV1hhU3VoTzdNZTZ4V3p4Zm5Jd2E0LVcyQTBNNjJ5VldmMHRfaGdNU0FVcDBSekVZTGJYUTRvbmVpd1IxNDBCSWJTT0FIclMwdktv?oc=5" target="_blank">Citywide implementation of a rapid whole-genome sequencing program for critically ill pediatric patients</a>  <font color="#6f6f6f">Nature</font>

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Clinical and genetic analysis of multiple mitochondrial dysfunctions syndrome type 6 caused by biallelic PMPCB variants in children
Frontiersworld

Clinical and genetic analysis of multiple mitochondrial dysfunctions syndrome type 6 caused by biallelic PMPCB variants in children

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPbWd5ZDE4emo0Tmx2YmhLNFZvQ0IxRlRqOVNFeUlXdEZBR2QyT1pFalExTmlsN095Vkdqck9ZdUl4LWU2dGhhbXpZU3Y2cHcwdnNFbVBrVF9pR3F6OWJCRlU3YUxuN2tlNUp3aXhhYTNvbjdSS3VHUUF0TlBPay1zeDVPa29pZ0JkSXRnVGJFaVo?oc=5" target="_blank">Clinical and genetic analysis of multiple mitochondrial dysfunctions syndrome type 6 caused by biallelic PMPCB variants in children</a>  <font color="#6f6f6f">Frontiers</font>

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/Using the power of AI to make genetic diagnosis easier: MARRVEL-MCP
Texas Children'stech

/Using the power of AI to make genetic diagnosis easier: MARRVEL-MCP

<a href="https://news.google.com/rss/articles/CBMinAFBVV95cUxNcU1jSnFkSlVJVWw5MEJUUXF3Z1F0OVA3NUxFdkZudGFlYVp3enV3eDYyVXFWTUItS3p5Z2RkTWdIWVQ2YWQ1cXVUd2VNRWdHSTZDWDdFcmVjQjJkUUMzaWZhY2JXTUE3UDZtOEhFYW40cXNkTnpLM2VLNnltUGVodlFxR3NPOUJBR09SRTI1QnlEMW13dVBYb3RPamc?oc=5" target="_blank">/Using the power of AI to make genetic diagnosis easier: MARRVEL-MCP</a>  <font color="#6f6f6f">Texas Children's</font>

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Pharmacogenetics in pediatric cardiology
Frontiersgeneral

Pharmacogenetics in pediatric cardiology

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPRzVQV0xaaXZEb1VYMWdKcXBlSE9FbEVYdUZuUzdlQ2FPNWVCRjV2VmVEQVlJTTJtSDd5ZVA3eENZejhadTRhd1lteFExQmhzQWJNY19Xai1OdWtqQ1JrOEZJcy1tUWhyaUxZSDg4Z1Q5bHo3M3dnczNVVzJ5V1Nja29SNmRxVnpKUmN2SkEwaE4?oc=5" target="_blank">Pharmacogenetics in pediatric cardiology</a>  <font color="#6f6f6f">Frontiers</font>

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Can Newborn Genetic Testing Identify Cancer Predisposition Genes?
The ASCO Postgeneral

Can Newborn Genetic Testing Identify Cancer Predisposition Genes?

<a href="https://news.google.com/rss/articles/CBMipgFBVV95cUxQNF83M0ZVS29jWlFFMnpoUkNRSnV2WEFzSUVVV1owdXpxR3cwR3BrckYtdlBYOEQ1aHR3RXFTZjRKU3pQMWhJM0FHYTVIVHlkYjhuWXB0OHpvYXdIanI2Y2NHQmNvVEpOVGdnemRqX1NMTGs5MkczNnFVT00xdGxsSkk3RURiZDZXZWczUGZES19CVzJmM1d6WTJud0pBdUZ2UlNjZktB?oc=5" target="_blank">Can Newborn Genetic Testing Identify Cancer Predisposition Genes?</a>  <font color="#6f6f6f">The ASCO Post</font>

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Genomic alterations in pediatric tumors: clinical relevance and translational insights
Naturegeneral

Genomic alterations in pediatric tumors: clinical relevance and translational insights

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFB6UDZfZDV6WE5nRWFmM3Z5Q3FwSVBsR0k1SkNLc042c0UxYV9yekNBRnBSOW5xQ3VTc1l3XzJnQnhUNW9OdWx0UXlUV1hHZ2poUUJsdWZMNmRiekFGZXUw?oc=5" target="_blank">Genomic alterations in pediatric tumors: clinical relevance and translational insights</a>  <font color="#6f6f6f">Nature</font>

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Why Genetics Should Guide Treatment for Pediatric Paragangliomas
University of Miamigeneral

Why Genetics Should Guide Treatment for Pediatric Paragangliomas

<a href="https://news.google.com/rss/articles/CBMid0FVX3lxTE96ZE9vU21sbUJyRzViczJoTTFld3lQQzlqN2tqMTVubG1QU0pIY1VoRzFoUWtNLVNoa1A4bTFLa0FZaThaOURYUDVqeTJQemhjMFJrNkQtWU9CYVpoZjFrVFBOUHJnT285a0trUEl0bWxXTXFlZUxR?oc=5" target="_blank">Why Genetics Should Guide Treatment for Pediatric Paragangliomas</a>  <font color="#6f6f6f">University of Miami</font>

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Case Report: Genetic testing reveals Wilson disease with familial hypertriglyceridemia in a 12-year-old boy
Frontiersgeneral

Case Report: Genetic testing reveals Wilson disease with familial hypertriglyceridemia in a 12-year-old boy

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPNWx4cUdwam42Nk81Y0t6dndfZ204cFdlZkcwUm5pYlJsRC1qbldXRXNsY1E2Y3Z6emVRLVFMTURHMEprRGEyRkJ3STFmWnkxZzd3MVQ3MzdnNmRBSlhsYWRKZXRKam5GNy1WV0lYMFZ4SnN1eEJnVmk0NVBMaWxnZnQxYkcxbW1FTXQyQUpfbTA?oc=5" target="_blank">Case Report: Genetic testing reveals Wilson disease with familial hypertriglyceridemia in a 12-year-old boy</a>  <font color="#6f6f6f">Frontiers</font>

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Challenges in identifying paediatric cancer predisposition syndromes: international SCOPE survey and SIOPE expert consensus recommendations | European Journal of Human Genetics
Natureworld

Challenges in identifying paediatric cancer predisposition syndromes: international SCOPE survey and SIOPE expert consensus recommendations | European Journal of Human Genetics

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFB0ckprdzlObE1fZWFSUzk2anA2Q205QWl1eHB6amFtY0pjUzNrZlpha2I2aG9aMjZwYTZ4T1RvU3JUODhUeTVNV2UzM1FVWlN2RGZMNUhlUTctLXlzZDdV?oc=5" target="_blank">Challenges in identifying paediatric cancer predisposition syndromes: international SCOPE survey and SIOPE expert consensus recommendations | European Journal of Human Genetics</a>  <font color="#6f6f6f">Nature</font>

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Institute for Pediatric Rare Diseases at FSU, A.J. Anderson Foundation expand access to genetic screening and rare disease care
Florida State University Newsworld

Institute for Pediatric Rare Diseases at FSU, A.J. Anderson Foundation expand access to genetic screening and rare disease care

<a href="https://news.google.com/rss/articles/CBMiiwJBVV95cUxOODdyQ2pISDJiMzF1VVpWaGNFV25tM1ZiMWNwUUNwU1JrN3U1UmRoVV92SHFyajJUclJ0N1ZVbjRlSnpjckp2ZkZ0OFMzZnZ6eVh4NVRvVjdNdl9WZ1ZyUXJLNU5JeVd4MFVyT3JQVGZ0c0tBX3hHMDBDX2M4ZG5RV0RrSFg0cVlCU2ZFTXlfQ3VCdlcxclA3enFiWnd2QmtvWWZ4US1sT1pteWdqcDVxTFl2bGxhTkdnc2FtV2puQ0haMUNlbExEMmdNUjZjZUM2aHVNN1dFMVpJQWdqeXgyZzdpcDBRaUZPb0U5VnRWV1pBM3lnT2l5TzRES1U2dmdZSkNJUkN0LWptUUk?oc=5" target="_blank">Institute for Pediatric Rare Diseases at FSU, A.J. Anderson Foundation expand access to genetic screening and rare disease care</a>  <font color="#6f6f6f">Florida State University News</font>

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New clinical framework maps pediatric Behçet’s spectrum disorders
News-Medicalgeneral

New clinical framework maps pediatric Behçet’s spectrum disorders

<a href="https://news.google.com/rss/articles/CBMiugFBVV95cUxPdkc2NHRXNjhoeFNMQmI4VnNQbFcyTklaVVVFOVRtcnZic2ZyZGFSZEVvNThQd1F6cUtIS1V4a1VhLWdySnplekYtdDgza05pUGNpYzdEd1JNRjAyR3F6WlJKMnRlSmRCWXAxRXVxOVFFVmo2V05HQmR6d05zdzZNS0dBRjNSeTJwd2RYczV4bV9oTGVZdTVFcXBXdXRxU1pMWmNKUDMzWlp0U3o1OWRuTXdyV1hMMVFvYkE?oc=5" target="_blank">New clinical framework maps pediatric Behçet’s spectrum disorders</a>  <font color="#6f6f6f">News-Medical</font>

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"Pediatric Genetic Testing" — Live Google News Trends & Headlines