1. Facial Features of Hereditary Cancer Predisposition
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2. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz–Jeghers syndrome
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3. A Novel AMELX Mutation, Its Phenotypic Features, and Skewed X Inactivation
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4. Peutz‑Jeghers syndrome: Skin manifestations and endocrine anomalies (Review)
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5. Black and Brown: Non-neoplastic Pigmentation of the Oral Mucosa
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6. Implications of Splicing Alterations in the Onset and Phenotypic Variability of a Family with Subclinical Manifestation of Peutz–Jeghers Syndrome: Bioinformatic and Molecular Evidence
   Andrea Cerasuolo et al, 2020, International Journal of Molecular Sciences CrossRef
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