The neonatal presentation of Prader-Willi syndrome revisited
- 1 February 1999
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 134 (2) , 226-228
- https://doi.org/10.1016/s0022-3476(99)70420-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationAmerican Journal of Medical Genetics, 1997
- Genetic and clinical advances in Prader-Willi syndromeCurrent Opinion in Pediatrics, 1996
- Diagnostic test for the Prader-Willi syndrome by SNRPN expression in bloodThe Lancet, 1996
- Muscle histochemistry in the Prader-Willi syndromeBrain & Development, 1994
- Prader‐Willi syndrome: Current understanding of cause and diagnosisAmerican Journal of Medical Genetics, 1990
- NEONATAL RESPIRATORY DEPRESSION AND DELAY IN DIAGNOSIS IN PRADER‐WILLI SYNDROMEDevelopmental Medicine and Child Neurology, 1989
- Recurrence risk in Prader-Willi syndromeAmerican Journal of Medical Genetics, 1987
- Pathology of muscular hypotonia in the Prader-Willi syndrome: Light and electron microscopic studyJournal of the Neurological Sciences, 1969