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Publications by Giampiero Igli Baroncelli
Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Paternal and Maternal Transmission of Pseudohypoparathyroidism Type Ia in a Family With Albright Hereditary Osteodystrophy: No Evidence of Genomic Imprinting.
Journal of Medical Genetics
Genetics
Genetic Deficiency of the Alpha Subunit of the Guanine Nucleotide-Binding Protein Gs as the Molecular Basis for Albright Hereditary Osteodystrophy.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance
Frontiers in Endocrinology
Endocrinology
Metabolism
Diabetes
Hemifacial Spasm in Albright''s Hereditary Osteodystrophy With Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus
Neurologia Medico-Chirurgica
Surgery
Neurology
The Prenatal Diagnosis of Hereditary Disorders
American Journal of Public Health
Environmental
Public Health
Occupational Health
The Prenatal Diagnosis of Hereditary Disorders
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer
PLoS ONE
Multidisciplinary
Association of the GNAS1 Gene Variant With Hypertension Is Dependent on Alcohol Consumption.
Hypertension Research
Internal Medicine
Cardiovascular Medicine
Physiology
Cardiology
Molecular Characterization of the Ribosomal RNA Gene Region of Perkinsus Atlanticus: Its Use in Phylogenetic Analysis and as a Target for a Molecular Diagnosis
Parasitology
Animal Science
Zoology
Parasitology
Infectious Diseases
