Comparison of perinatal factors in deletion versus uniparental disomy in Prader–Willi syndrome

Author:

Gold June‐Anne12,Mahmoud Ranim13,Cassidy Suzanne B.14,Kimonis Virginia1ORCID

Affiliation:

1. Division of Genetics and Genomic Medicine, Department of PediatricsUniversity of CaliforniaIrvine California

2. Division of Genetics and Metabolism, Department of PediatricsLoma Linda UniversityLoma Linda California

3. Genetics Unit, Department of Pediatrics, Faculty of MedicineMansoura UniversityMansoura Egypt

4. Division of Medical Genetics, Department of PediatricsUniversity of CaliforniaSan Francisco California

Funder

Center for Scientific Review

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome

2. Benefits and limitations of prenatal screening for Prader-Willi syndrome

3. Prader-Willi syndrome

4. Center for Disease Control and Prevention. (1980–2003).Vital Statistics of the United States: 1980–2003. Retrieved fromhttps://www.cdc.gov/nchs/products/vsus/vsus_1980_2003.htm

5. Does the genetic cause of Prader‐Willi syndrome explain the highly variable phenotype?;Dobrescu A. I.;Maedica (Buchar),2016

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