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Publications by J.M. Pina-Neto

Lack of Evidence for Monosomy 1p36 in Patients With Prader-Willi-Like Phenotype

Brazilian Journal of Medical and Biological Research

English

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Schaaf-Yang Syndrome Shows a Prader-Willi Syndrome-Like Phenotype During Infancy

Orphanet Journal of Rare Diseases

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Deletion of the SIM1 Gene (6q16.2) in a Patient With a Prader-Willi-Like Phenotype

Journal of Medical Genetics

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Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome

Frontiers in Endocrinology

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Prader-Willi Syndrome

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Atypical Presentation of Juvenile Rheumatoid Arthritis in a Patient With Monosomy 1p36

Annals of Paediatric Rheumatology

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Prader-Willi Syndrome

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The Role of the Prader-Willi Syndrome Critical Interval for Epigenetic Regulation, Transcription and Phenotype

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Exploring Autism Symptoms in an Australian Cohort of Patients With Prader-Willi and Angelman Syndromes

Journal of Neurodevelopmental Disorders

Cognitive Neuroscience

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Prader-Willi Syndrome in a Child With XYY

Journal of Human Genetics

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