A New Inherited Syndrome With Cardiac, Cutaneous, and Endocrine Involvement
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference3 articles.
1. Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes;McKusick,1983
2. The complex of myxomas, spotty pigmentation, and endocrine overactivity;Carney;Medicine (Baltimore),1985
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1. The Role of Genetic and Epigenetic Changes in Pituitary Tumorigenesis;Neurologia medico-chirurgica;2014
2. Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients and 80 Different Genotypes;The Journal of Clinical Endocrinology & Metabolism;2009-06-01
3. Familial endocrine myxolentiginosis;Clinical Cardiology;1995-11
4. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991
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