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Publications by V.R. Rodríguez

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

Brazilian Journal of Medical and Biological Research
ImmunologyCell BiologyPharmacologyBiochemistryBiophysicsNeuroscienceMedicineToxicologyPhysiologyPharmaceutics
2008English

Related publications

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

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2019English

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

Journal of Medical Genetics
Genetics
2002English

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

Frontiers in Endocrinology
EndocrinologyMetabolismDiabetes
2019English

Prader-Willi Syndrome

2020English

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

Annals of Paediatric Rheumatology
2014English

Prader-Willi Syndrome

English

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

Epigenomes
2018English

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

Journal of Neurodevelopmental Disorders
PediatricsCognitive NeurosciencePerinatologyNeurologyForensic MedicineChild HealthPathology
2018English

Prader-Willi Syndrome in a Child With XYY

Journal of Human Genetics
Genetics
1999English

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