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Carney complex
To View the ESE Recommended Curriculum of Specialisation in Clinical Endocrinology, Diabetes and Metabolism
RD-Action Matchmaker – Summary of Disease Expertise Recorded Under
Multiple Orbital Neurofibromas, Painful Peripheral Nerve Tumors, Distinctive
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Identification of HRAS Mutations and Absence of GNAQ Or GNA11
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Blueprint Genetics Comprehensive Growth Disorders / Skeletal
Blueprint Genetics Comprehensive Skeletal Dysplasias and Disorders
Hypotyreose V01
Exome Sequencing Identifies PDE4D Mutations As Another Cause of Acrodysostosis
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The Complex of Myxomas, Spotty Skin Pigmentation and Endocrine Overactivity (Carney Complex): Imaging Findings with Clinical and Pathological Correlation
Carney Complex” an Often [1]
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Top View
A Case of Myhre Syndrome Mimicking Juvenile Scleroderma Barbara Jensen1*, Rebecca James2, Ying Hong1, Ebun Omoyinmi1, Clarissa Pilkington3, Neil J
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Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging
G Protein Mutations in Endocrine Diseases
Mutations in the Protein Kinase a R1α Regulatory Subunit Cause Familial Cardiac Myxomas and Carney Complex
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Familial Brain Tumour Syndromes
Tumors Associated with Carney Complex, Carney Triad and Carney-Stratakis Syndrome
Genetics of Endocrinology
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Multiple Endocrine Neoplasia Syndromes Glenda G
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Carney Complex: an Update 173:4 M85–M97 Special Section Review
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Carney Complex
Tumoral Phenocopies of Hypertrophic Cardiomyopathy: the Role of Cardiac Magnetic Resonance
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MAPK Activation and HRAS Mutation Identified in Pituitary Spindle Cell Oncocytoma
Rare Genetic Disorders Test Requisition Form
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A Mouse Model for the Carney Complex Tumor Syndrome Develops Neoplasia in Cyclic AMP–Responsive Tissues
Familial Thyroid Cancer: a Review
Heart Myxoma Develops Oncogenic and Metastatic Phenotype
Rare Mendelian Disorders Test Requisition Form
The Lentiginoses: Cutaneous Markers of Systemic Disease and a Window to New Aspects of Tumourigenesis
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Loss of Prkar1a Leads to Bcl-2 Family Protein Induction and Cachexia in Mice
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Fed Pract. 2020;37(Suppl 4):S82-S88. Doi:10.12788/Fp.0033 1 APC Familial Adenomatous Polyposis-1 AD Predisposition to Cancer
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Joel L. Spitz, Editor. Genodermatoses. a Clinical Guide to Genetic Skin Disorders
University of California, San Diego
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Pediatrische Oncopredispositie Panel Versie V1 (195 Genen) Centrum Voor Medische Genetica Gent
Primary Cardiac Tumors Associated with Genetic
Disease ID Disorder Name Gene Symbols OMIM ID