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Publications by Pietro Chiurazzi
A Novel Gene, FAM11A, Associated With the FRAXF CpG Island Is Transcriptionally Silent in FRAXF Full Mutation
European Journal of Human Genetics
Genetics
A Unique Case of Reversion to Normal Size of a Maternal Premutation FMR1 Allele in a Normal Boy
European Journal of Human Genetics
Genetics
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FMR3 Is a Novel Gene Associated With FRAXE CpG Island and Transcriptionally Silent in FRAXE Full Mutations
Journal of Medical Genetics
Genetics
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia
Reproductive Sciences
Gynecology
Obstetrics
A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
Nuclear Medicine
Radiology
Oral Surgery
Imaging
Dentistry
Forensic Medicine
Pathology
Surgery
A Novel Mutation in CELSR1 Is Associated With Hereditary Lymphedema
Vascular Cell
Computer Networks
Developmental Neuroscience
Neurology
Cell Biology
Communications
PDCD4gene Silencing in Gliomas Is Associated With 5′CpG Island Methylation and Unfavourable Prognosis
Journal of Cellular and Molecular Medicine
Molecular Medicine
Cell Biology
A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Novel NKX2.1 Mutation Associated With Hypothyroidism and Lethal Respiratory Failure in a Full-Term Neonate
Journal of Perinatology
Gynecology
Child Health
Pediatrics
Perinatology
Obstetrics
A Nonsense Mutation (E1978X) in the ATM Gene Is Associated With Breast Cancer
Breast Cancer Research and Treatment
Cancer Research
Oncology
MAPT Promoter CpG Island Hypermethylation Is Associated With Poor Prognosis in Patients With Stage II Colorectal Cancer
Cancer Management and Research
Oncology