Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients

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

(2018) June-Anne Gold et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome

(2018) Preeti Singh et al.   JOURNAL OF MEDICAL GENETICS

Global epidemiology of use of and disparities in caesarean sections

(2018) Ties Boerma et al.   LANCET

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

(2017) Céline Bar et al.   Orphanet Journal of Rare Diseases

Benefits and limitations of prenatal screening for Prader-Willi syndrome

(2016) Merlin G. Butler   PRENATAL DIAGNOSIS

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings

(2015) M. A. Angulo et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Prader-Willi syndrome can be diagnosed prenatally

(2014) Noa Gross et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A population-based profile of 160 Australians with Prader-Willi syndrome: Trends in diagnosis, birth prevalence and birth characteristics

(2014) Tess Lionti et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prader-Willi syndrome

(2012) Suzanne B. Cassidy et al.   GENETICS IN MEDICINE

Maternal age effect on the development of Prader–Willi syndrome resulting from upd(15)mat through meiosis 1 errors

(2011) Keiko Matsubara et al.   JOURNAL OF HUMAN GENETICS

Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

(2008) A. P. Goldstone et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Pre-, peri- and postnatal complications in Prader–Willi syndrome in a UK sample

(2007) J.E. Whittington et al.   EARLY HUMAN DEVELOPMENT