Segmental Isodisomy in Prader–Willi Syndrome Patients: The Experience of a Single Diagnostic Center

Pediatrics and Neonatology - Singapore
doi 10.1016/j.pedneo.2020.02.007
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

Prader-Willi Syndrome

2020English

Prader-Willi Syndrome

English

Diagnostic Testing for Prader-Willi Syndrome and Angelman Syndrome: A Cost Comparison

Genetics in Medicine
MedicineGenetics
2002English

Detection of Aberrant DNA Methylation in Unique Prader — Willi Syndrome Patients and Its Diagnostic Implications

Human Molecular Genetics
MedicineGeneticsMolecular Biology
1994English

Prader-Willi Syndrome Association UK

2018English

Functional Neuroimaging in Prader–Willi Syndrome

International Journal of Obesity
NutritionEndocrinologyDieteticsMedicineMetabolismDiabetes
2006English

Hypotonia and Prader Willi Syndrome in the Neonatal Period

Genetics in Medicine
MedicineGenetics
1999English

Deaths Due to Choking in Prader–Willi Syndrome

American Journal of Medical Genetics, Part A
Genetics
2007English

Perinatal Features of Prader-Willi Syndrome: A Chinese Cohort of 134 Patients

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy